Short-Term Fasting Synergizes With Solid Cancer Therapy By Boosting Antitumor Immunity
Mar 10, 2023
Simple Summary:
Stimulating our body’s immune response to fight cancer is important for the success of cancer treatment in general. To further improve current cancer therapy, preclinical research shows that short-term fasting diets enhance cancer therapy efficacy, such as chemotherapy. Short-term fasting diets are low-caloric and low in protein for 3–5 days; they are usually done every couple of weeks. This review summarizes preclinical and clinical evidence of fasting diets synergizing with cancer therapy by boosting antitumor immunity.
After research, it was found that the extract of Cistanche deserticola is rich in immunity and anti-cancer effects. The Institute of Biochemical Engineering, Department of Chemical Engineering, Tsinghua University has developed a new technology for the production of phenylethanoid glycosides by Cistanche cell culture, applied for a national invention patent for this technology, and completed the large-scale cell culture process and the separation of phenylethanoid glycosides Purification research, increase the content of phenylethanoid glycosides (total glycosides) to about 10% of the dry cell weight.
Abstract:
Short-term fasting (STF), using a low-caloric, low-protein fasting-mimicking diet (FMD), appears to be a promising strategy to enhance chemotherapy-based cancer efficacy, while potentially alleviating toxicity. Preclinical results suggest that enhanced tumor immunity and decreased growth signaling, via lowering of circulating insulin and insulin growth factor 1 (IGF-1) levels form the potential underlying mechanisms. STF may boost anti-tumor responses by promoting tumor immunogenicity and decreasing local immunosuppression.
These findings warrant further studies focused on the combination of STF, not only with chemotherapy but also with immunotherapy to evaluate the full range of benefits of STF in cancer treatment. Here, we delineate the underlying anticancer mechanisms of fasting. We summarize preclinical evidence of STF boosting antitumor immunity and alleviating immunosuppression, as well as the clinical findings reporting the immunomodulatory effects of STF during various cancer treatments, including immunotherapy.
Keywords:
short-term fasting; fasting-mimicking diet; cancer therapy; immunomodulation; cancer immunity; chemotherapy; immunotherapy
1. Introduction
The nature of the local immune response is strongly associated with the success of different cancer treatments [1,2]. Short-term fasting (STF) as an adjunct to cancer treatment can reinforce tumor immunity and, therefore, boost the efficacy of chemo- and immunotherapy. The potential underlying mechanisms are increased immunogenicity of the tumor and alleviated tumor- and/or chemotherapy-induced immunosuppression [3,4]. Pre-clinical studies have well-established the benefits of adding fasting to cancer therapy [5]. These include the protection of healthy cells from chemotoxicity while sensitizing tumor cells to chemotherapy at the same time, resulting in delayed progression [3,5,6]. An increasing number of clinical trials provide evidence for the benefits of STF in the treatment of cancer, including the reduction of chemotoxicity [6–9].
In recent studies, the anticancer effects of fasting were also attributed to improved antitumor immunity [3,4,10,11]. These findings suggest that fasting can reinforce the antitumor response when combined with chemotherapy, and encourage further exploration of combinations with other treatments, immunotherapy for instance.
Over the last century, preclinical studies have documented the health benefits of continuous restriction of daily caloric intake by 30–60% compared to ad libitum intake [12,13].
However, continuous calorie restriction is difficult to sustain. That is why current research focuses on the biological and clinical effects of STF as a more feasible alternative. Water-only fasting is safe for many weeks in healthy people [6,14] but is arguably even more difficult than continuous calorie restriction. Therefore fasting mimicking diets (FMDs) were designed to mimic its molecular physiological effects, while still allowing the consumption of (low-calorie) food, primarily comprising of complex carbohydrates and healthy fatty acids [15]. FMDs are low-caloric and low-protein diets comprising roughly 200–1100 kcal per day for 3–5 days, often repeated in cycles every couple of weeks. Intermittent fasting may be defined as short (1–2 days) periods of fasting or low caloric intake separated by 1–5 days of usual food consumption [12]. Periodic fasting is usually defined as 4 or more consecutive days of low-calorie intake, separated by weeks to months of regular consumption. Time-restricted eating entails restriction of eating for a time window of roughly between 6 and 10 h a day. Time-restricted eating is not primarily meant to restrict intake and can be isocaloric too [16]. Dietary restriction refers to the reduction or omission of specific groups of nutrients.
Finally, calorie restriction mimetics are worth mentioning since these drugs are designed to mimic the caloric restriction effects pharmacologically while still allowing regular diet consumption [17]. Here, we mainly focus on studies evaluating the effects of intermittent/periodic fasting and FMD but sometimes refer to results from other fasting modules. It is important to note that different fasting diets might have distinct effects in the context of cancer or antitumor immunity.
Antitumor immunity is known to be crucial to the success of any cancer treatment [1,2]. It is determined by the balance between immunogenicity and immune evasion by tumor cells [3,18]. At the start of neoplastic transformation, cancer cells elicit an immune response, driven by cytotoxic cells of the innate immune system, such as natural killer cells, neutrophils, and cytotoxic macrophages, as well as by cytotoxic CD8+ T cells from the adaptive immune system. CD4+ T cells play a supportive role in the cytotoxic attack. Unfortunately, less immunogenic cancer cells survive and are positively selected, also known as clonal selection or evolution. As the tumor progresses and evolves, more complex immune evasion maneuvers occur, involving corruption of the surrounding stromal tissue to induce local immunosuppression in the tumor microenvironment.
This narrative review will delineate the proposed underlying mechanisms of fasting. Next, preclinical evidence to support that STF promotes antitumor immunity and alleviates immunosuppression will be summarized, as well as clinical findings on STF-induced immunomodulation during various cancer treatments, including immunotherapy. Lastly, obstacles, current gaps in the literature, and future directions of research will be discussed.
2. Methods
A literature search was performed in the PubMed database to systematically collect literature for this narrative review, which yielded 136 results on 6 November 2021, and was routinely checked until 10 December 2021. The terms fasting, caloric restriction, immune system phenomena, immune modulation, and neoplasm were used among others, as shown in the search strategy displayed in Supplementary File S1. At first, the selection was based on title screening, abstract information, and type of publication. The articles were included if cancer and cancer therapy were the main focus. As a result, 28 articles were selected as summarized in Figure 1. Relevant references from these articles were collected using the snowballing method.
2.1. Fasting Causes Metabolic Reprogramming, Stimulates Autophagy, and Can Increase Immunogenic Cell Death
Fasting causes nutrient shortage on a systemic level, which results in metabolic reprogramming and induces autophagy on a cellular level via nutrient sensing pathways [15Interestingly, fasting differentially affects healthy cells compared to tumor cells. On the one hand, fasting increases the resistance of healthy cells to stressors, a phenomenon called differential stress resistance (DSR) (6,7,19） On the other hand, it sensitizes tumor cells to stressors, known as differential stress sensitization [5,7,19]. As a result, fasting can lead to a form of cell death known as immunogenic cell death (ICD) in response to chemotherapy radiation(5，20）
ICD is a specific type of cell death that often evokes an antitumor immune response (21)Some chemotherapies are known to induce ICD, such as mitoxantrone and oxaliplatin (22,23）During ICD, tumor cells secrete adenosine 5'-triphosphate (ATP) and calreticulin among other surface proteins (24). ATP, in particular, promotes the recruitment of dendritic cells (DCsto the tumor bed (24), and calreticulin stimulates tumor antigen absorption by DCs (21)Consequently, increased DC infiltration can lead to increased antigen presentation and subsequently elicit a tumor-specific immune response.
STF induces metabolic reprogramming by systemically lowering several nutrient hormones' plasma concentrations, such as glucose, insulin, and insulin growth factor 1IGF-1). Directly downstream of the IGF-1 receptor (IGF-1R), the nutrient-sensing pathway mammalian target of rapamycin (mTOR) integrates cell growth signals with metabolic and environmental cues via phosphoinositide 3-kinase (PI3K) and protein kinase B (Akt oi)[15.25-271.Therefore.AKdecreased lhplasma concentration downregulates ICF-IR-AKT-mTOR and cyclic adenosine monophosphate protein kinase A (CAMP-PKA) signalingDecreased mTOR pathway signaling warns the cell about resource shortages and induces metabolic reprogramming to survive by lowering metabolic demand and switching cell metabolism towards other energy sources, such as fatty acids [5,19]. Lowered metabolic and mitotic activity can potentially hamper cellular uptake of chemotherapeutic toxins and limit intracellular damage induction in healthy cells (5,191. It is this crucial metabolic switch through which fasting affects tumor cells and healthy cells differentially.
Tumor cells are less able to adapt to STF-induced nutrient shortage [5,19]. This is because most tumor cells rely on anaerobic glycolysis for ATP production, known as the Warburg effect (28,29]. This increased metabolic state requires abundant energy and building blocks in the form of glucose and glutamine to support tumor growth and proliferation among other tumorigenic properties [30]. Even when oxygen is available and their mitochondria are functional, tumor cells do not use mitochondrial oxidative phosphorylation to harvest energy in the form of ATP [29]. STF appears to induce an anti-Warburg effect in tumor cells, characterized by a switch to oxidative phosphorylation and increased oxygen consumption [26,31]. During this anti-Warburg effect, some studies observed increased accumulation of reactive oxygen species (ROS) and apoptosis [31]. Indeed, STF renders tumor cells more vulnerable to other stressors, such as chemotherapy [5,19].
Healthy cells are metabolically rewired upon fasting to induce autophagy, stimulate internal repair processes, and protect against the toxic effects of chemotherapy [6, 7,19,21,26,32]. STF induces autophagy at least partially through mTOR downregulation. Autophagy is a lysosomal degradation process that plays an important role in cell survival in response to virtually any kind of stress, including starvation. It eliminates damaged organelles, misfolded proteins, and invading pathogens. The breakdown products can be used as fuel and/or building blocks for starved cells [15,26]. Autophagy also forces the cell to prioritize internal repair mechanisms and it may prevent malignant transformation in the long run [15,26,33]. On top of that, autophagy balances the production of ROS, contributing to cell protection against damage by free radicals [26]. Interestingly, a growing body of evidence suggests that autophagy has a substantial role in the extension of a life and health span induced by caloric restriction [33].
STF directly induces autophagy in tumor cells as well [26]. The role of autophagy in cancer is complex. It sometimes stimulates tumor progression, depending on the type and stage of tumor development [34]. In contrast, there is also evidence that autophagy can inhibit tumor growth, partially by depleting tumor cells of acetyl-CoA and ATP [17], which renders them more vulnerable to chemotherapy [35]. Moreover, perhaps even more importantly, autophagy contributes to ICD [5,7,21,24]. Thus, the role of autophagy in cancer (treatment) is complex and remains to be fully elucidated [21,34,35].
In summary, STF can protect healthy cells against the side effects of chemotherapy, while simultaneously sensitizing tumor cells to cancer therapy. These benefits are mainly achieved through metabolic reprogramming and stimulating autophagy. Consequently, there is an increased ICD of tumor cells, which may result in enhanced antitumor immunity.
2.2. Pre-Clinical Evidence Shows That STF Can Decrease Immunosuppression and Boost Antitumor Immunity
Several preclinical studies have investigated the immunomodulating mechanisms of fasting, using different fasting diets, as shown in Table 1 [3,4,36]. Here, we will focus on T cells and macrophages, and we elaborate on how fasting affects their metabolism, decreases immunosuppression, promotes regeneration, and ultimately boosts antitumor immunity, as illustrated in Figure 2.
T cell metabolism is affected by STF in various short- and long-term ways. Short-term STF has negative effects on effector T cells, as they rely on glycolysis for their high metabolic demand. Consequently, effector T cells have a harder time competing with cancer cells in the tumor microenvironment for nutrients during STF [41]. Low glucose conditions are linked to increased transcription of genes that render T cells dysfunctional [42]. Nevertheless, T cells with increased glycolytic activity characterized by heightened mTOR pathway signaling can show low persistence, antigen recall response, and proliferative capacity [39–41]. Conversely, inhibiting mTOR signaling with rapamycin was shown to increase T-cell persistence [43].
In the long term, CD8+ and memory T cells can adapt to nutrient restriction [44]. STF increases adenosine monophosphate-activated protein kinase (AMPK) pathway activity, which can promote long-term survival and lineage stability through fatty acid oxidation [44,45]. Furthermore, T cells with low metabolic activity show increased persistence and increased proliferative capacity later on [46]. Moreover, Sukumar et al. showed that T cells with low metabolic activity, used in adoptive transfer therapy of a melanoma mouse model, mediate a better antitumor response, evidenced by increased T cell proliferation and better tumor control among other things [47]. Therefore, fasting diets pose an interesting way of reducing mTOR- and increasing AMPK signaling to improve T cell-mediated antitumor responses in the long term.
Figure 2.
Immunomodulatory mechanisms of short-term fasting [STF] during anticancer therapy. STF reduces immunosuppression and enhances antitumor immunity via the following mechanisms established from preclinical studies: CD73 downregulation in cancer cells causes decreased adenosine release, which in turn diminishes immunosuppressive M2-type macrophage polarization. Decreased heme oxygenase-1 (HO-1) production by cancer cells (and M2 macrophages) releases inhibition of regulatory T (Tregs) cells on CD8+ cytotoxic T cells directly as well as direct inhibition from HO-1. Lowered glycolysis inhibits macrophage and granulocyte colony-stimulating factor (M-CSF, G-CSF) secretion by cancer cells. Consequently, fewer myeloid-derived suppressor cells are mobilized from the bone marrow. Hematopoietic stem cell regeneration of common lymphoid progenitors (CLP), naïve T cells, and accumulation of memory T cells is observed centrally. A peripheral increase of CD8+ and CD4+ T cells is observed after refeeding and might replenish exhausted T cells as well as increase tumor antigen recognition chance. Autophagy induction stimulates tumoricidal M1 macrophage differentiation, which can support antitumor immunity. Figure 2 is adapted from “Cancer Immunoediting”, by BioRender.com (2022).
In addition, effector T cells experience less immunosuppression by regulatory T cells (Tregs) during STF as shown in Figure 2 [48]. A preclinical study observed Treg depletion (CD4+, CD25+, Foxp3+) during calorie restriction mimetics (hydroxy citrate, an ATP citrate lyase inhibitor) in an autophagy-competent lung cancer (TC-1 non-small cell) mouse model treated with ICD-inducing chemotherapy (mitoxantrone or oxaliplatin) [3]. Moreover, this combination treatment improved tumor growth control in colorectal cancer and an MCA205 fibrosarcoma model as well. Furthermore, this compound effect required autophagy induction and was mediated by depleting Tregs frequency [3]. Interestingly, the hydroxy citrate-treated mice showed levels of autophagy induction similar to 48 h fasted mice [3]. Contrastingly the hydroxy citrate and cisplatin combination did not show improved outcomes in the MCA205 fibrosarcoma mouse model, perhaps because cisplatin elicits ICD only minimally [3,49]. Together, these results suggest that both STF and hydroxy citrate synergize with ICD-inducing chemotherapy to improve efficacy compared to single-agent or STF treatment alone.
Another mice study by Di Biase et al. showed a reduction in intra-tumoral Tregs in B16 melanoma and 4T1 breast cancer models after 4 days FMD every 2 weeks for 2–3 cycles in addition to chemotherapy [4]. This led to an increase of CD8+ tumor-infiltrating lymphocytes (TILs) and cytotoxicity in the tumor bed illustrated in Figure 2 and correlated with delayed tumor progression. Further analysis showed that the improved CD8+ infiltration and cytotoxicity were dependent on heme oxygenase-1 (HO-1) downregulation. HO-1 is an enzyme involved in the breakdown of free heme [50]. HO-1 is often described to modulate the tumor microenvironment in favor of tumor progression [51]. It is noteworthy that among other cells, Treg cells can express HO-1 to dampen T cell antitumor immunity [52], which makes HO-1 an interesting potential target for therapy.
Furthermore, Di Biase et al. found that T cells experience hematopoietic regeneration upon STF. The authors observed an increase in the common lymphoid progenitor count in the bone marrow accompanied by increased circulating naïve CD3+/CD8+ cells upon FMD [4]. This effect could theoretically aid specific antitumor T cell-mediated response [4], as this new pool of T cells may respond to previous or newly formed tumor antigens. Takakuwa et al. also observed an increase in naïve T cells (CD44−, CD8+, CD4+) in the bone marrow of mice after 48 h of fasting [37].
Other investigators, using caloric restriction of 50% for 6 weeks continuously in mice models, reported remodeling of the bone marrow compartment as well [38], specifically accumulation of memory T cells. A reduction in CD4+ and CD8+ T cells within the peripheral blood and the secondary lymphoid organs was observed as well. Lymphocyte redistribution commenced after 1 week of caloric restriction and remained stable for at least 6 weeks. CD4+ and CD8+ T cell numbers significantly increased in bone marrow after 3 weeks of caloric restriction. The central memory T cell accumulation in bone marrow during caloric restriction was associated with enhanced tumor immunity and survival benefit in mice receiving melanoma-specific CD8+ T cells after a melanoma tumor challenge at 3 weeks of energy restriction [38].
Additionally, Cheng et al. observed hematopoietic stem cell regeneration effects in mice that fasted for 48–120 h around cyclophosphamide chemotherapy for six cycles in 12–14 days. The hematopoietic stem cell regeneration was dependent on the downregulation of IGF-1/PKA signaling, an important endocrine sequel of fasting [39]. Moreover, mortality due to chemotherapy was significantly reduced (p < 0.01) in mice fasted for 48 h (n = 10) compared to ad libitum-fed mice (n = 10).
In contrast, the tumor-promoting myeloid-derived suppressor cells (MDSCs) do not benefit from hematopoietic regeneration [40]. One study showed that the MDSC (CD11b+, Gr1+) frequency was similar in peripheral blood mononuclear cells (PBMCs) but reduced in the spleen after two cycles of 4-day FMD (with 50% or 70% calorie restriction) followed by a 10-day ad libitum diet in a 4T1 breast cancer mouse model [40]. Moreover, a significant reduction of tumor-resident MDSCs and an increased T cell to MDSC ratio in PBMCs was detected [53].
Similar results were achieved in a study using intermittent fasting in 4T1 and 4T07 preclinical tumor models, where the decreased accumulation of granulocytic MDSCs in the spleen was associated with reduced tumor growth [54]. Another study showed that glycolysis reduction by 2-deoxy-D-glucose inhibited granulocyte- and macrophage colony-stimulating factor production by tumor cells, which resulted in less mobilization of MDSC in the 4T1 preclinical model as visualized in Figure 2 [55]. This effect was associated with improved T-cell immunity, tumor growth inhibition, and prolonged survival [55].
After MDSCs are mobilized by tumor cells, they can differentiate into the heterogenous group of tumor-associated macrophages (TAMs) [56]. During FMD, these macrophages differentiate less effectively into an M2 phenotype, which is immunosuppressive TAMs [36,57]. A study in colorectal cancer models demonstrated that upon FMD, CD73 expression by tumor cells is reduced and this blunts adenosine releases into the extracellular environment, thereby preventing the JAK1/STAT3 signaling-dependent shift towards M2 macrophages [36]. The polarization of macrophages towards an M1-tumoricidal phenotype rather than an M2-immunosuppressive phenotype might be mediated through autophagy [58]. Fasting can induce autophagy (at least partially) via the reduction of mTOR signaling. Therefore, FMD-induced downregulation of mTOR could partially similarly alleviate TAM-driven immunosuppression as mTOR and PI3K targeting agents can modulate macrophage-induced immunosuppression [57,59]. Modulation of TAMs by fasting through these mechanisms is an interesting strategy since the tumor microenvironment comprises up to 50% of TAMs in some solid tumors and high levels of TAMs are associated with adverse prognosis [57,60].
Interestingly, some of the M2-like TAMs display an increased expression of HO-1 that can dampen antitumor immunity [50,61,62]. High levels of HO-1 expression in tumor or stromal cells are associated with anti-apoptotic effects as well as therapy resistance and poor prognosis [63]. Preclinical studies have explored targeting HO-1 in anticancer therapy. For instance, Alaluf et al. showed that myeloid-specific HO-1 deletion led to enhanced antigen-specific CD8+ cytotoxicity upon therapeutic immunization in the thymoma (EG7/OVA) mouse model [50].
Another study shows that the use of tin mesoporphyrin to inhibit HO-1 expression in immunosuppressive TAMs (fibroblast activation protein alpha+) in tumor-bearing mice (LL2/OVA) allowed for better tumor growth control [61]. Muliaditan et al. used tin mesoporphyrin in combination with 5-fluorouracil to reverse immunosuppression by myeloid-derived HO-1 activity in a spontaneous breast cancer mouse model [62]. Additionally, immunological tumor growth control was superior compared to immune checkpoint inhibition, possibly due to enhanced CD8+ T cell effector function [62]. Therefore, targeting HO-1 with FMD might be a promising strategy to reduce immunosuppression and enhance antitumor immunity [4,26], considering these results.
2.3. Clinical Studies on Fasting Combined with Cancer Treatment
Clinical trials have shown beneficial effects of STF in cancer treatment, such as a reduced increase in DNA damage in PBMCs after chemotherapy administration [8,9,11,64–67] and reduction of clinical side effects and possibly improved quality of life (QoL), as shown in Table 2 [8,65]. It is important to note that these studies are small and should be validated by larger trials.
At first, a case series by Safdie et al. reported on patients (n = 10) diagnosed with different types of cancers, who water-only fasted for 48–140 h before chemotherapy and/or 5–56 h following chemotherapy [9]. Patients were under their control, as some chemotherapy cycles were accompanied by fasting and others were not. Six out of ten patients reported fewer chemotherapeutic side effects, such as less fatigue, weakness, and gastrointestinal issues, when fasting. One patient experienced reduced myelosuppression. These results suggest that STF can relieve chemotherapy-induced toxicity.
Similar results were reported by Dorff et al. in another feasibility trial. Twenty patients with diverse malignancies were divided into three groups, water-only fasted for (1) 24 h or (2) 48 h prior, or (3) 48 h before and 24 h (72 h total) after platinum-based chemotherapy [66]. Moreover, ≥48 h of fasting tended to be associated with reduced DNA damage in leukocytes (p = 0.08) assessed by COMET assay. There was also a non-significant trend toward less grade 3 or 4 neutropenia in the 48 and 72-h cohorts compared to the 24-h fasting cohort (p = 0.17).
Moreover, Bauersfeld et al. found indications that water-only fasting for 60 h around chemotherapy administration was associated with a higher QoL score and experiencing less fatigue in 34 patients with gynecological cancer [65]. In this small crossover trial, patients were randomized to fast during the first half of chemotherapy cycles, followed by a regular diet during the second half, or vice versa (NCT01954836).
A randomized pilot study by de Groot et al. (NCT01304251) included 13 early-stage breast cancer patients, half of whom water-only fasted for 24 h before and after chemotherapy [67]. Results suggested that water-only fasting might diminish the induction and/or speed up the recovery of chemotherapy-induced DNA damage in healthy PBMCs, as assessed by y-H2AX intensity in CD45+ and CD3+ T lymphocytes [66]. These results indicate that fasting might protect healthy cells from chemotherapy-induced DNA damage [66,67].
This inference is supported by the results of our randomized phase 2 DIRECT trial (DIetary REstriction as an adjunct to neoadjuvant ChemoTherapy for HER2-negative breast cancer), which included randomized patients between FMD and regular diets 3 days before and on the day of neoadjuvant chemotherapy, showing that FMD reduced DNA damage in T-lymphocytes after chemotherapy administration as compared to the regular diet arm (p = 0.045) [8].
Although the study had to be aborted halfway for practical and statistical reasons, a complete or partial radiological response of the tumor occurred more often in patients receiving FMD (OR 3.168; CI 1.062–9.446; p = 0.039). Furthermore, the per-protocol analysis of the pathological response revealed that a 90–100% tumor cell loss was more likely to occur in the FMD group (OR 4.109; 95% CI 1.297–13.02; p = 0.016). We observed no difference in grade 3 or 4 toxicity between the two treatment arms, although it is worth noting that dexamethasone to alleviate toxicity was omitted in the FMD arm. Finally, QoL and illness perception domains appeared to improve in patients receiving FMD [68]. To build upon these results, we are preparing the DIRECT2 trial to validate results in a larger patient group (grants awarded).
Recently, Vernieri et al. published the results of an observational trial evaluating the impact of a 5-day FMD cycle every 3–4 weeks in patients (n = 101) with various types of cancer [11]. A flow cytometry analysis of PBMCs (n = 38) revealed a reduction of peripheral MDSCs subsets (CD14+ HLA-DRneg, CD14+ programmed cell death protein 1 ligand+ (PD-L1) and CD15+) and CD3+ CD25+ T cells after each FMD cycle.
Furthermore, FMD induced an increase in cytolytic natural killer (NK) cell activity as well as a boost in CD4+ and CD8+ TIL activity defined by programmed cell death protein 1 (PD-1) and CD69 co-expression. These observations were accompanied by altered intra-tumoral immune composition, more specifically numbers of CD8+ T cells, and activated DCs and NK cells were increased, as well as by systemically interferon gamma activating immune signatures that are generally associated with better prognosis in cancer. In a subset of 18 breast cancer patients undergoing surgery, the resection sample showed a significant decline in IGF-1R staining and increased CD8+ TILs compared to the paired pre-FMD biopsy.
Moreover, RNA-seq data analyses of transcriptomic signatures suggested an increase in M1-type macrophages, whereas M2 macrophages did not change significantly after FMD. These findings were supported by immunohistochemistry of CD8+ TILs, CD68+ cells, Perforin 1, granzyme B, IGF-1R, and phosphor-IGF-1R. In concert, these data support the theory that fasting boosts antitumor immunity and calls for further investigation of the antitumor efficacy of fasting in larger randomized clinical trials.
2.4. Fasting Can Synergize with Other Cancer Therapies, including Endocrine, Radiation, and Immunotherapy
Several translational studies combined fasting with cancer treatment modalities other than chemotherapy, such as endocrine therapy, radiation therapy, immunotherapy, and targeted therapy [10,69–71].
Caffa et al. hypothesized that fasting could support endocrine therapy since 75% of all breast cancers are hormone receptor-positive (HR+) and IGF-1 and insulin signaling through the PI3K-Akt-mTOR axis enhance the activity of this hormone receptor resulting in endocrine resistance [69]. The authors demonstrated that FMD boosts the effectiveness of fulvestrant and tamoxifen in an HR+ breast cancer mouse model, via upregulation of early growth response 1 (EGR1), which coincided with decreased PI3K-Akt-mTOR signaling.
Furthermore, the authors showed that cyclin-dependent kinase 4/6 inhibitor palbociclib combined with fulvestrant and periodic FMD cycles led to prolonged tumor control and reversed acquired drug resistance in vivo (n = 18). These observations were validated in patients with HR+ breast cancer (n = 36) who received a variety of endocrine therapies. Lowered levels of circulating insulin, IGF-1, and leptin were measured after an average of 5–6 FMD cycles of 5 days in a feasibility trial. These metabolic changes persisted for 1–3 weeks after FMD for IGF-1 and leptin. Four patients received endocrine therapy and palbociclib combined with FMD and showed promising results, such as longer progression-free survival [69].
Manukian et al. studied the immunomodulatory effects of caloric restriction in triple-negative breast cancer in mice treated with radiation therapy (RT) [70]. While RT promoted ICD, it also increased the percentage of CD4+ CD25+ Foxp3+ T cells among TIL. In contrast, the CD8+ T cells to Treg ratio in the TILs was increased four-fold in calorie-restricted mice (1.11% in the RT group vs. 4.2% in the calorie-restricted + RT group; p < 0.002). Caloric restriction-induced tumor control was at least partially mediated by CD8+ T cells, as their anti-CD8- antibody-induced depletion during caloric restriction resulted in rapid tumor outgrowth and decreased median survival. Moreover, PD-1 expression was increased in tumor-infiltrating CD3+ CD8+ T cells immunofluorescence analysis in calorie-restricted mice compared to mice fed ad libitum, which likely reflects enhanced activation of T cells.
Indeed, tumor immunity was boosted and Treg numbers declined in mice receiving RT accompanied by calorie restriction [70]. Notably, early-stage breast cancer patients undergoing RT while receiving 75% of baseline diet calories (n = 28) were reported to show signs of reduced systemic immunosuppression, defined as decreased serum levels of IL2-receptor γ, IL10 receptor β, TGF-β2, and TGF-β3, when compared to patients treated with RT only (n = 10) [70].
An experimental study in non-small cell lung cancer with several syngeneic tumor models demonstrated that short-term starvation for 48–72 h sensitizes tumor cells to immune checkpoint blockade with antibodies against PD-1 [10]. Short-term starvation and anti-PD-1 immunotherapy inhibited the progression and metastasis of breast- and melanoma cancer. This antitumor effect was dependent on CD8+ cells. Additionally, the treatment combination increased the intra-tumoral CD8+/Treg ratio and boosted tumor-specific immunity.
Conversely, the authors report that anti-PD-1/ therapeutic resistance is associated with high plasma levels of IGF-1 or high tumor IGF-1 receptor expression in non-small-cell lung cancer patients, which by extension suggests that lowering IGF-1 through STF could be beneficial. In another preclinical mouse model, Lévesque et al. employed a triple strategy of ICD-inducing chemotherapy (mitoxantrone and oxaliplatin) combined with fasting or calorie restriction mimetics (hydroxy citrate or spermidine) and immune checkpoint inhibitors targeting the interaction between PD-1 and its ligand [71]. This strategy cured most of the tumor-bearing mice by establishing T cell-dependent control of tumor growth, while ICD-inducing chemotherapy without fasting or calorie restriction mimetics sensitized the tumor only modestly to treatment with PD-1 blockade alone [71].
These translational results demonstrate the synergistic potential of combining chemoimmunotherapy with fasting regimens. Taken together with the evidence supporting the immunomodulating effects of STF, clinical trials investigating the combination of fasting or FMDs with (chemo-) immunotherapy or targeted therapy are warranted.
3. Discussion
Preclinical studies showed that STF as an adjunct to various cancer therapies can potentially improve antitumor immunity, by decreasing immunosuppression and enhancing CD8+ cytotoxicity. Additionally, STF stimulates hematopoietic stem cell regeneration and accumulation of memory T cells in the bone marrow compartment in drug-treated cancer mouse models, which was associated with increased numbers of naïve T cells in some studies [4,38,72]. Moreover, a fasting-induced decrease in tumor-induced immunosuppression was associated with a better prognosis in vivo. These findings make a strong case for synergism between fasting and other cancer therapies. Several translational studies have successfully explored the synergistic potential of combinations with chemoimmunotherapy, targeted-, radiation-, and endocrine therapy. Future research can build on these cornerstones.
A beneficial impact of STF on the adverse effects of chemotherapy has been observed in several clinical trials [9,65]. In keeping with these observations, dexamethasone omission did not increase the side effects in breast cancer patients receiving FMD in the DIRECT trial, despite the toxicity of anticancer agents [8]. In addition, PBMCs had less chemotherapy-induced DNA damage in these patients, suggesting that FMD protected against chemotoxicity [8]. These findings support the DSR paradigm, which predicts that healthy cells and tissues are better protected against chemotoxicity by STF [6,19]. Finally, our DIRECT trial showed some beneficial effects of adding FMD to neoadjuvant chemotherapy on clinical response [8]. Nevertheless, further research is needed to validate the preclinical findings, as well as the preliminary positive clinical effects of STF on anticancer therapy.
Compliance remains a challenge for fasting in clinical practice. Variations in dietary options and taste, as well as support by a nutritionist or dietician, could help. Future studies should incorporate these and other measures to optimize compliance. Patients will be even more motivated to adhere to the dietary rules once evidence of efficacy has been confirmed as it did preclinically. Lastly, a better understanding of STF and FMD on the immune system and antitumor immunity is required. We are currently initiating the FIND study (the effect of a Fasting mimickINg Diet on the immune system: an exploratory study; NCT04833439) to examine the immunomodulatory effects of FMD in healthy individuals in depth, using the RNA NanoString analysis on PBMCs collected before and after two cycles of a 4-day FMD. The outcomes of this small explorative trial will help to better understand the direction of the immunomodulating effects of FMD, which in turn will aid in the setup of future clinical trials, such as the DIRECT-2 trial (expected recruiting in 2022).
4. Conclusions
In pre-clinical models, STF can support antitumor immunity by increasing immunogenicity and relieving immunosuppression. This evidence warrants clinical trials investigating the combination of fasting or STF with chemoimmunotherapy and other cancer treatment modalities, examining STF's effects on the immune system. In the future, large phase 3 clinical trials are essential to evaluate if and for which types of cancer therapy STF enhances the therapeutic efficacy.
5. Key Messages
• Preclinical evidence shows that STF can reduce adverse events and improve the antitumor effects of chemotherapy.
• Preclinical evidence demonstrates that STF can potentiate antitumor immunity, in part by enhancing immunogenicity and relieving tumor-induced immunosuppression.
• Clinical trials show that short-term fasting around chemotherapy is safe in a select group of fit patients and may increase the effectiveness of chemotherapy
• (Pre-)clinical evidence suggests fasting regimens might alleviate the immunosuppressive effects of chemotherapy.
• More studies are required to confirm that STF boosts the efficacy of cancer therapy, such as chemotherapy and immunotherapy, by enhancing tumor immunity.
Author Contributions:
All authors contributed to the preparation of this manuscript. Writing— original draft and editing, N.d.G.; visualization—figure and table, N.d.G.; writing—review and editing, J.R.K., H.P., and S.H.v.d.B. All authors have read and agreed to the published version of the manuscript.
Funding:
This research received no external funding.
Conflicts of Interest:
The authors declare no conflict of interest.
Abbreviations
AKT, Akt protein kinase B
AMPK adenosine monophosphate-activated protein kinase
ATP adenosine 50 -triphosphate
cAMP-PKA cyclic adenosine monophosphate protein kinase A
CLP common lymphoid progenitor
CP cyclophosphamide
CR complete response
CT chemotherapy
DC dendritic cells
DSR differential stress resistance
DXR doxorubicin
ECM extracellular matrix
EGR1 early growth response 1
FMD fasting-mimicking diet
G-CSF granulocyte colony-stimulating factor
HER2 human epidermal growth factor receptor 2
HO-1 heme oxygenase-1
HR+ hormone receptor-positive
ICD immunogenic cell death
IFNγ interferon gamma
IGF-1 insulin growth factor 1
IGF1R insulin growth factor 1 receptor
M-CSF macrophage colony-stimulating factor
MDSC myeloid-derived suppressor cells
mTOR mammalian target of rapamycin
MTX mitoxantrone
NK natural killer cell
OX oxaliplatin
PBMC peripheral blood mononuclear cell
PD1 programmed cell death protein 1
PD-L1 programmed cell death protein 1 ligand
PI3K phosphoinositide 3-kinase
PR partial response
QoL quality of life
ROS reactive oxygen species
RT radiation therapy
STF short-term fasting
TAC docetaxel/doxorubicin/cyclophosphamide
TAM tumor-associated macrophages
TIL tumor-infiltrating lymphocyte
Tregs regulatory T cells
References
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