
Cancer is considered one of the most important causes of death, because it is a fatal malignancy. Cancer is the second leading cause of mortality in the world, with an estimated 9.6 million deaths in 2018 according to a World Health Organization (WHO) report. The most fatal types of cancer that cause serious deaths are lung, prostate, colorectal and stomach cancer. Cancer is caused by DNA damage, deficiency in DNA repair, or genomic instability leading to uncontrolled cell growth and tumor formation (Sung et al., 2021). Current chemotherapy for cancer comes with a variety of undesirable side effects such as diarrhea, bone marrow suppression, peripheral neuropathy and cardiotoxicity (Gegechkori et al., 2017). Therefore, researchers are investigating innovative treatments and preventive measures for cancer.
Postbiotics are metabolic products secreted by probiotics which are live bacteria such as Lactobacillus (L.) and Bifidobacterium (B.), using prebiotics as a nutrient source such as dietary fiber and oligosaccharides (Nataraj et al., 2020). Probiotics are living microorganisms that metabolize in the gut and provide health benefits (Batista et al., 2020). Recently, research on postbiotics utilizing these advantages has been actively conducted. Postbiotics have been reported to have health-promoting effects such as immunomodulation, anti-carcinogenic, hypolipidemic, and antihypertensive characteristics (Fang et al., 2014; Aguilar-Toalá et al., 2020; Engevik et al., 2021). More recently, postbiotics have emerged as an alternative to probiotics for high-risk patients or patients with underlying diseases who have difficulty using live probiotic strains. Postbiotics are considered potential anticancer agents due to their properties such as known chemical structure, safe profile, longer shelf life, nontoxicity, resistance to hydrolysis and stability to digestive system conditions compared to probiotics (Nataraj et al., 2020).
Currently, anti-cancer reviews mainly focus on probiotics and colorectal cancer. However, the present review fully addresses the importance of postbiotics in various cancer types. Several reports have suggested that postbiotics exhibit anticancer activity through anti-proliferative, apoptotic, and anti-inflammatory effects. Consequently, it provides a basic understanding of the alternative cancer treatment and mechanisms of postbiotics.
Probiotics are living microorganisms that are beneficial to health by using prebiotics as nutrients, a type of dietary fiber, to secrete postbiotics (Batista et al., 2020). Postbiotics are bioactive soluble factors secreted from probiotics or released during the fermentation and lysis of bacteria. They provide physiological benefits to the host as metabiotics, biogenics, or simply metabolites. Before the term postbiotics appeared in 2018, researchers referred to them as “biogenic,” “cell-free supernatant,” “abiotic,” “metabiotic,” “paraprobiotic,” “ghost probiotics,” “pseudoprobiotic,” “postbiotic,” supernatant,” etc. (Aguilar-Toalá et al., 2018). Postbiotics consist of bacteriocins, enzymes, vitamins, amino acids, neurotransmitters, short-chain fatty acids (SCFAs), nitric oxide (NO), organic acids, etc., which have been reported to have immune, antioxidant, and anticancer effects and regulate lipid/cholesterol metabolism (Bönisch et al., 2018; Hati et al., 2019).
The composition and activity of the gut microbiota in the host depends on the nutrients provided by the host (Asnicar et al., 2021). Furthermore, these microbes secrete a myriad of metabolites that contribute to the growth of beneficial organisms, interaction of cells, and promoting production. These interactions by metabolites are vital for shaping host-microbial symbiosis and the establishment of stable communities via modulation of cellular metabolism. Bacterial lysis occurs during the production of postbiotics, releasing other intracellular metabolites and various compounds as follows (Fig. 1); SCFs (acetate, butyrate, propionate, lactate), proteins/peptides (bacteriocin, glutathione, lactocepin), vitamins (biotin, riboflavin, pantothenate, ascorbic acid, thiamine, folic acid, phylloquinone, cobalamin), enzymes (GPx, SOD, peroxidase), cell wall components (lipoteichoic acid, teichoic acid peptidoglycan-derived, S-layer), and carbohydrates (polysaccharide, galactose) (Hati et al., 2019). Butyrate, a host energy source, is mainly used by intestinal epithelial cells, and acetate is used systemically (Venegas et al., 2019). Acetate and propionate move to the liver and peripheral organs and become substrates for gluconeogenesis and lipogenesis.
Postbiotics are produced naturally through the fermentation of probiotics, and the various biological properties of postbiotics depend on different production environment conditions (Homayouni Rad et al., 2021). As shown in Fig. 1, in addition to natural methods, pure postbiotics with high functionality are produced by physical methods including mechanical disruption, heat treatment, UV irradiation, formalin inactivation, high hydrostatic pressure, freeze-drying, sonication, filtration, ohmic heating, supercritical CO2, pulsed electric field, pH changes and drying (Barros et al., 2021). In general, heat treatment is the most useful method, and a variety of methods are used to improve the nutritional value, shelf life and health functionality for consumers.
Before discussing the therapeutic benefits of postbiotics, the issue of stability of postbiotics must be addressed. Probiotics treatment uses living microorganisms, which can cause problems due to the generation of antibiotic-resistant genes and virulence factors in vivo. This is especially important for young children with an immature immune system and weak barriers, and postbiotics can bypass this problem.
Seven randomized controlled trials (RCT) of 1,740 children reported that supplementation with heat-killed L. acidophilus LB reduced the duration of diarrhea and prevented pharyngitis, laryngitis, and diarrhea (Malagón-Rojas et al., 2020). Among the RTCs, only one showed dehydration associated with heat-killed L. acidophilus LB administration. It was confirmed that heat-inactivated L. acidophilus LB can activate immune-inflammatory mechanisms in children related to intestinal cell adhesion and pro-inflammatory chemokines. To evaluate the effect of L. paracasei CNCM I-1572 on intestinal microflora, a clinical study was conducted on children aged 6–14. As a result, it was reported that the function of the gut microbiota was modulated without adverse side effects (Cremon et al., 2018). Furthermore, Andresen et al. (2020) reported that heat-killed B. bifidum HI-MIMBb75 alleviated irritable bowel syndrome. The most common adverse event in this clinical trial was suspected abdominal pain occurring in two patients (< 1%) in the B. bifidum HI-MIMBb75 group and one patient (< 1%) in the placebo group. Further studies are necessary to determine the effects and side effects of various postbiotics.
Compared to probiotics, postbiotics have many advantages for industrial production, including ease of use and storage, extended shelf life, stability over a wide range of pH and temperature, and no bioamine production. Nevertheless, further studies on manufacturing, delivery systems and safety parameters of pharmaceuticals and functional foods are needed to utilize postbiotics as probiotic substitutes (Salminen et al., 2021).
In preclinical and clinical studies, carcinogens of nutritional origin, such as polycyclic aromatic hydrocarbons (PAH), N-nitroso compound (NOCs), heterocyclic amine (HCA), acrylamide, and mycotoxins, were found to cause breast cancer, colorectal cancer, liver cancer and prostate cancer (Wang et al., 2012). These substances promote uncontrolled cell growth and DNA damage in the mammary gland, colon and prostate (Hebels et al., 2010). In general, PAH components are absorbed by charcoal-grilled, smoked, and processed meats. In this regard, N-nitroso compounds, even in small amounts, can be harmful to the host and are directly related to digestive system cancer (Xu et al., 2015).
The gut microbiota directly or indirectly affects the host's tumorigenesis. Digestive system cancer, especially colorectal cancer, is caused by abnormalities of the intestinal bacteria and the proliferation of certain bacterial pathogens, such as Helicobacter (H.) pylori, Streptococcus (S.) bovis, Enterococcus faecalis, Clostridium septicum, Escherichia coli, Fusobacterium spp., Bacteroides fragilis, and Streptococcus gallolyticus (Li et al., 2019). Bacterial pathogens influence host intestinal commensal bacteria and immune system efficiency to induce tumor growth and development. Bacterial pathogens directly contribute to host tumorigenesis by releasing large numbers of toxins and regulating several cellular proliferation and promotion pathways (Mager, 2006). Typically, dysbiosis in the gut environment predominantly affects pathogenic bacteria, and destroys the host’s DNA through the production of toxins, leading to genomic instability, tumor initiation and progression (Sobhani et al., 2011). According to Wei et al. (2010), H. pylori as a class A carcinogen negatively regulates p53 by increasing ubiquitination and proteasomal degradation by activation of serine/ threonine kinase AKT, which phosphorylates and activates the ubiquitin ligase HDM2.
Recent in vitro and in vivo studies have reported that postbiotics have important anticancer effects (Table 1). In this review, the molecular mechanisms of postbiotics in cancer prevention and treatment are involved in pathways such as modulation of immune response, inhibition of mutagenesis and carcinogens, activation of pro-apoptotic pathways, decreased bacterial translocation, and increased apoptosis and autophagy.
Apoptosis of cancer cells determines the rate of cancer cell development. Postbiotics are of great interest to scientists because they cause the apoptosis of cancer cells without damaging adjacent cells. Postbiotics include modulating apoptosis signaling through mitochondrial-dependent (intrinsic) and death receptor-dependent (extrinsic) pathways (Fig. 2). Riaz et al. (2019) showed that the induction of intrinsic and extrinsic apoptosis of L. rhamnosus was achieved by the up-regulation of Bad, Bax, caspase3, caspase8, and caspase9, and down-regulation of Bcl-2 genes in human cervical cancer HeLa cells. Phagocytosis of S. cerevisiae in human breast cancer MCF7 cell is associated with the disruption of mitochondrial membrane potential and activation of initiator and effector caspases 8, 9, and 3 (Ghoneum and Gollapudi, 2004). It was demonstrated that postbiotics from L. paracasei IMPC2.1 and L. rhamnosus GG inhibit the growth and progression of human colon cancer DLD-1 cell and human gastric cancer HGC-27 cell lines through the activation of the pro-apoptotic pathway (Orlando et al., 2012). In addition, ferrichrome derived from L. casei has been reported to have an apoptotic effect on tumor cells through an increase in cleaved PARP and cleaved caspase 3 (Konishi et al., 2016).
Bacteriocin Laterosporulin10 extracted from Brevibacillus spp. has been reported to induce apoptosis of human cancer cells lines MCF-7, HEK293T, HT1080, HeLa and H1299 by in vitro flow cytometry analysis (Baindara et al., 2017). Jan et al. (2002) have suggested that propionibacteria inhibit human colorectal cancer cell lines HT-29 and caco-2 in vitro by their ability to produce SCFA inducing apoptosis. These studies show that bacterial culture supernatants and pure SCFA exhibited typical apoptosis, including loss of mitochondrial transmembrane potential, generation of reactive oxygen species, caspase-3 treatment, oncoprotein Bcl-2 regulation, and nuclear chromatin condensation. Based on this evidence, it is believed that certain postbiotics upregulate cancer cell proliferation inhibition and apoptosis pathways.
The cell cycle arrest of cancer cells suppresses cancer cell proliferation by controlling cell division. Cells continue to cycle in the sequence of G1, S, G2, and M phases, among which DNA replication occurs in S phase and cell division occurs in M phase (Fig. 2). The G1 and G2 phases are the stages to ensure that division and replication have completely occurred. Specific regulation between cyclin-dependent kinases (CDKs) and cyclins is important to the progression of the cell cycle. Cyclin D/CDK4 in G1 phase, cyclin A/CDK2 in S phase, and the cyclin B/CDC2 complex in G2/M phase are involved in cell cycle regulation, respectively.
Cell wall components, peptidoglycans, cytoplasmic extracts, and cell supernatants of various postbiotics exhibit antiproliferative effects against cancer cell lines. SCFAs produced in P. freudenreichii caused the accumulation of sub-G1 phase, and the reduction of S and G2/M phases in human colorectal cancer RKO cells, as measured by FACS (Casanova et al., 2018). It has been reported that cell-free pentasaccharide of L. spp. promotes apoptosis and inhibits S-phase cell cycle progression in human colorectal cancer HT-29 cell and primary colon cells T4056 (Elfahri et al., 2016). Hosseini et al. (2020) showed that nisin, the cytoplasmic extract of L. lactis ssp. lactis, and the cell walls of this bacterium have an antiproliferative effect that is associated with the decreased expression of cyclin D1 in human colorectal SW480 cancer cells in vitro. An et al. (2019) found that the antiproliferation activity of probiotic-derived p8 protein was mediated by inhibition of the p53-p21-Cyclin B1/Cdk1 signal pathway, resulting in growth arrest at the G2 phase of the cell cycle in vitro in human colorectal DLD-1 cells. Thus, it can be suggested that postbiotics inhibit the proliferation of cancer cells.
Autophagy is a cellular process that maintains intracellular homeostasis by delivering misfolded proteins and damaged organelles to lysosomes. Numerous studies have shown that increased autophagy in many cancer cells can inhibit tumorigenesis. A functional blockade of the proteasome induces high levels of GRP78, promoting autophagosome formation through activation of the unfolded protein response (UPR) in the endoplasmic reticulum stress pathway. Beclin-1 induces dissociation of the Beclin-1/Bcl-2 complex, thereby promoting autophagy by reducing the Beclin1/PI3K-III complex (Fig. 2).
Tang et al. (2011) have demonstrated that propionate treatment in human colon carcinoma cell lines HCT-116 and SW480 exhibit extensive characteristics of autophagic proteolysis by increased LC3-I to LC3-II conversion, acidic vesicular organelle development, and reduced p62/SQSTM1 expression. Kim et al. (2010) reported that cell-bound exopolysaccharides isolated from L. acidophilus 606 inhibited the proliferation of HT-29 colon cancer cells by directly affecting cell morphology. This anticancer activity is due to the activation of autophagic cell death, which is promoted not only indirectly through the induction of Bcl-2 and Bak, but also directly by the induction of Beclin-1 and GRP78. Therefore, autophagy of cancer cells is a useful approach in postbiotic cancer therapy.
A delicate balance between immune responses depends on the various mediators released by cancer cells, cancer-associated cells and host inflammatory cells in the tumor microenvironment. Thus, modulation of immune response determines the overall outcome of the carcinogenesis process. Activated macrophages and neutrophils eliminate tumor cells (Fig. 3). Moreover, anti-inflammatory and pro-apoptotic cytokines such as TRAIL, interleukin (IL)-10 and TGF-β inhibit carcinogenesis depending on the particular tumor microenvironment. Postbiotics upregulate the functioning of the gut immune system and the treatment and prevention of chronic inflammatory diseases (Żółkiexicz et al., 2020).
Kim et al. (2013) reported that SCFA activates GPR41 and GPR43 in intestinal epithelial cells, leading to mitogen-activated protein kinase signaling and the rapid production of chemokines and cytokines. These pathways mediate immunity and inflammation response in mice. Heat-killed L. gasseri TMC0356 reportedly has immunomodulatory effects through stimulation of IL-12 production in macrophages (Kawase et al., 2012). SCFA protects the mucosal layer from damage by reducing the levels of immunomodulators, such as prostaglandin, produced by cyclooxygenase 2 (COX-2), which induce tumor inflammation and development in human breast cancer MCF7 cells (Nakkarach et al., 2021). Therefore, postbiotics have the same effective immunomodulatory activity as live probiotics, and the optimal level of the inactivation method (mainly the method of preparation by heat treatment) may not adversely affect the immunomodulatory and anti-inflammatory properties. Heat-killed
L. pentosus b240 promoted the production of immunoglobulin A (IgA), IL-6, IL-10, interferon (IFN)-γ, and tumor necrosis factor, but not IL-4, IL-5, B-cell activating factors, IFN-α, IFN-β, and transforming growth factor-β1 (Kotani et al., 2014). L. plantarum strain YYC-3 strongly inhibited human colorectal cancer HT-29 and Caco2 cell lines. This anticancer effect involved a mechanism that modulated the immune system and downregulated the expression of inflammatory cytokines interleukin IL-6, IL-17, and IL-22, along with reduced infiltration of inflammatory cells (Yue et al., 2020). Based on these results, studies using cell lines demonstrated that postbiotics had anticancer effects through immunomodulation, suggesting that postbiotics-based therapies can be used for anticancer treatment.
Under normal conditions, enterocytes in the intestinal wall are a key defense mechanism for maintaining the entire intestine. The gastric mucosal layer protects against destruction of the intestinal epithelium by unsafe compounds. An important component of the intestinal barrier is the mucus layer, which contains various mucin glycoproteins that maintain homeostasis and regulate the inflammatory response (Fig. 3). The gut environment contains many different types of bacteria that coexist in balance with the host. Various in vitro studies have demonstrated that SCFA has a protective effect on DNA transcription and has the potential to protect the intestinal barrier by inhibiting histone deacetylase (HDAC), which regulates gene expression and increases the expression of MUC2 in goblet cells (Hatayama et al., 2007). Several studies have reported that SCFA enhances epithelial cell tight junctions by stimulating 5-adenosinmonophosphate (5’-AMP) to activate protein kinase, a fundamental role in regulating energy metabolism in colon cells. According to a report by Zheng et al. (2017), microbial-derived butyrate enhanced IEC barrier formation, induced IL10RA mRNA, IL-10RA protein, and transactivation through activated Stat3 and HDAC inhibition. It has been demonstrated that P40, a soluble protein derived from L. rhamnosus GG, promotes the intestinal barrier by activating EGFR and synthetic mucin (Wang et al., 2014). Consequently, postbiotics are effective in the prevention and treatment of colorectal cancer by preserving the intestinal barrier.
Many pathogens have shown to cause human cancer. Studies have reported associations between H. pylori and stomach cancer, bovis streptococci and colorectal cancer, Chlamydia pneumonia and lung cancer, Salmonella and gallbladder cancer, respectively (Mager, 2006). The gut microbiota greatly affects the health of the host. The intestinal environment is pH 5.5–6.5; the upper large intestine is a weakly acidic pH environment, and in the lower large intestine, the pH is more neutral. The growth of bacterial pathogens is reduced when the intestinal pH is below 6.0 and the panel cells release antimicrobial peptides (Kok et al., 2020). A diet supplemented with heat-killed Limosilactobacillus fermentum and L. delbrueckii promotes the growth of beneficial B. spp. and associated metabolic changes in the human fermented fecal community (Warda et al., 2021). SCFAs keep the human gut environment at pH 5–6, inhibiting harmful bacteria and allowing beneficial bacteria to thrive (Kok et al., 2020). Kotani et al. (2014) showed that L. rhamnosus GG lowered the activity of β-glucuronidase to inhibit the dehydration and oxidation of bile acids, thereby inhibiting microbial enzymes. Moreover, L. plantarum b240 prevented bacteria pathogens from invading and adhering to the intestinal epithelial cell surface. A diet using postbiotics has the potential to alter gut microbiota composition, diversity, and richness (Kotani et al., 2014).
Cancer destroys the intestinal barrier and immune system during oncogenesis as well as concurrently with anticancer therapy. The research presented in this review demonstrates the biological response including beneficial health effects and protection of the intestinal barrier through the metabolites contained in postbiotics. Various mechanisms explain the prevention and treatment of postbiotics in cancer. Several studies have shown that postbiotics have anticancer effects by inhibiting apoptosis, proliferation, and autophagy of cancer cells. Therefore, this paper aims to develop postbiotics that have fewer side effects and better cancer treatment effects. Additional metabolomic studies are needed to characterize novel postbiotics and investigate safety parameters, anticancer properties, stability during the food manufacturing process, marketing, and gut status. Randomized, double-blind clinical trials are also needed to determine the appropriate dosage and optimal frequency of administration of supplements for cancer patients. In the future, it will be possible to perform anticancer treatment with the selected postbiotics.
암 발병률의 급격한 증가와 기존 암 치료에 따른 부작용과 합병증으로 인해 포스트바이오틱스를 이용한 암 치료에 대한 연구가 증가하고 있다. 포스트바이오틱스는 비활성화된 미생물 세포, 세포 분획 또는 대사 산물과 같은 광범위한 생리 활성 인자이며 숙주에게 다양한 생리학적 건강상의 이점을 제공한다. 포스트바이오틱스는 고위험 환자 또는 살아있는 프로바이오틱 균주를 사용하기 어려운 기저 질환이 있는 환자를 위한 프로바이오틱스의 대안이 될 수 있으며 긴 유통기한, 무독성 및 소화 계통에 대한 안정성 등의 특성을 지닌다. 포스트바이오틱스는 세포 사멸, 항증식 및 항염증 효과를 통해 항암 효과를 나타낼 뿐만 아니라 장내 미생물 및 면역 체계의 구성을 조절한다. 이를 통해 포스트바이오틱스가 부작용 없고 효과적인 새로운 항암제 후보 물질임을 시사한다. 이 논문은 암 예방 및 치료에 대한 포스트바이오틱스의 생물학적 역할을 강조하면서 포스트바이오틱스를 둘러싼 개념 및 안전성 문제에 대한 개요를 제공한다.
None.
The authors have no conflict of interest to report.
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