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Erschienen in: Journal of Gastrointestinal Cancer 2/2020

26.04.2019 | Review Article

Gut Microbiota as a Positive Potential Therapeutic Factor in Carcinogenesis: an Overview of Microbiota-Targeted Therapy

Erschienen in: Journal of Gastrointestinal Cancer | Ausgabe 2/2020

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Abstract

Cancer therapeutic methods comprising chemotherapy, radiotherapy, and surgery are so routine in cancer treatment. Remarkably, there are several personal features which affect the effectiveness of such treatments including nutrition, microbiome diversity, and physical activity which has distinct significant roles during and after therapies along with their bilateral connections. In this way, the ability of gut microbiota36 in modulating the efficacy of chemotherapeutic medications in cancer and other types of disorders is of great importance. In addition, the role of dietary, probiotic, and synthetically engineered bacteria in manipulating and optimizing the gut microbiota is of interest. Conspicuously, the correlation between the commensal microbiota and also host can regulate the physiological activities comprising the immunity system and inflammatory agents and it is scanned in the category of cancers. Bacterial species have been employed in cancer therapy; commensal microbes posse a key beneficial role in this field. Practically, the microbiota has this potential to accelerate and modulates a certain response by priming in order to release the pro-inflammatory agents. We would like to discuss these vital factors in this review as gut microbiota has the potential to be the main option for personalized cancer treatment strategies in the future. Meaning, this novel data present clinical promising feasibilities of modulating cancer therapy with using microbiota.
Literatur
1.
Zurück zum Zitat Tomayko E, Pillsbury L, Pray L. The human microbiome, diet, and health: workshop summary. Washington, D.C: National Academies Press; 2013. p. 196. Tomayko E, Pillsbury L, Pray L. The human microbiome, diet, and health: workshop summary. Washington, D.C: National Academies Press; 2013. p. 196.
15.
Zurück zum Zitat Goroll AH, Mulley AG. Primary care medicine: office evaluation and management of the adult patient. Philadelphia: Lippincott Williams & Wilkins; 2012. 1613 P. Goroll AH, Mulley AG. Primary care medicine: office evaluation and management of the adult patient. Philadelphia: Lippincott Williams & Wilkins; 2012. 1613 P.
16.
17.
Zurück zum Zitat Wells N, Pasero C, McCaffery M. Improving the quality of care through pain assessment and management. In: Hughes RG, editor. Patient safety and quality: an evidence-based handbook for nurses. Rockville (MD): Agency for Healthcare Research and Quality (US); 2008. Chapter 17. Available from: https://www.ncbi.nlm.nih.gov/books/NBK2658/. Wells N, Pasero C, McCaffery M. Improving the quality of care through pain assessment and management. In: Hughes RG, editor. Patient safety and quality: an evidence-based handbook for nurses. Rockville (MD): Agency for Healthcare Research and Quality (US); 2008. Chapter 17. Available from: https://​www.​ncbi.​nlm.​nih.​gov/​books/​NBK2658/​.
20.
Zurück zum Zitat Nouri Z, Karami F, Neyazi N, Modarressi MH, Karimi R, Khorramizadeh MR, et al. Dual anti-metastatic and anti-proliferative activity assessment of two probiotics on HeLa and HT-29 cell lines. Cell J. 2016;18(2):127.PubMedPubMedCentral Nouri Z, Karami F, Neyazi N, Modarressi MH, Karimi R, Khorramizadeh MR, et al. Dual anti-metastatic and anti-proliferative activity assessment of two probiotics on HeLa and HT-29 cell lines. Cell J. 2016;18(2):127.PubMedPubMedCentral
24.
Zurück zum Zitat Muti P, Bradlow HL, Micheli A, Krogh V, Freudenheim JL, Schünemann HJ, et al. Estrogen metabolism and risk of breast cancer: a prospective study of the 2: 16α-hydroxyestrone ratio in premenopausal and postmenopausal women. Epidemiology. 2000;11(6):635–40.CrossRefPubMed Muti P, Bradlow HL, Micheli A, Krogh V, Freudenheim JL, Schünemann HJ, et al. Estrogen metabolism and risk of breast cancer: a prospective study of the 2: 16α-hydroxyestrone ratio in premenopausal and postmenopausal women. Epidemiology. 2000;11(6):635–40.CrossRefPubMed
25.
Zurück zum Zitat Lombardi P, Goldin B, Boutin E, Gorbach SL. Metabolism of androgens and estrogens by human fecal microorganisms. J Steroid Biochem. 1978;9(8):795–801.CrossRefPubMed Lombardi P, Goldin B, Boutin E, Gorbach SL. Metabolism of androgens and estrogens by human fecal microorganisms. J Steroid Biochem. 1978;9(8):795–801.CrossRefPubMed
32.
Zurück zum Zitat Bronte V, Chappell DB, Apolloni E, Cabrelle A, Wang M, Hwu P, et al. Unopposed production of granulocyte-macrophage colony-stimulating factor by tumors inhibits CD8+ T cell responses by dysregulating antigen-presenting cell maturation. The Journal of Immunology. 1999;162(10):5728–37.PubMed Bronte V, Chappell DB, Apolloni E, Cabrelle A, Wang M, Hwu P, et al. Unopposed production of granulocyte-macrophage colony-stimulating factor by tumors inhibits CD8+ T cell responses by dysregulating antigen-presenting cell maturation. The Journal of Immunology. 1999;162(10):5728–37.PubMed
34.
Zurück zum Zitat Bronte V, Apolloni E, Cabrelle A, Ronca R, Serafini P, Zamboni P, et al. Identification of a CD11b+/Gr-1+/CD31+ myeloid progenitor capable of activating or suppressing CD8+ T cells. Blood. 2000;96(12):3838–46.CrossRefPubMed Bronte V, Apolloni E, Cabrelle A, Ronca R, Serafini P, Zamboni P, et al. Identification of a CD11b+/Gr-1+/CD31+ myeloid progenitor capable of activating or suppressing CD8+ T cells. Blood. 2000;96(12):3838–46.CrossRefPubMed
37.
Zurück zum Zitat Blumen H, Fitch K, Polkus V. Comparison of treatment costs for breast cancer, by tumor stage and type of service. Am Health Drug Benefits. 2016;9(1):23.PubMedPubMedCentral Blumen H, Fitch K, Polkus V. Comparison of treatment costs for breast cancer, by tumor stage and type of service. Am Health Drug Benefits. 2016;9(1):23.PubMedPubMedCentral
42.
Zurück zum Zitat Lewandowska U, Szewczyk K, Owczarek K, Hrabec Z, Podsędek A, Sosnowska D, et al. Procyanidins from evening primrose (Oenothera paradoxa) defatted seeds inhibit invasiveness of breast cancer cells and modulate the expression of selected genes involved in angiogenesis, metastasis, and apoptosis. Nutr Cancer. 2013;65(8):1219–31. https://doi.org/10.1080/01635581.2013.830314.CrossRefPubMed Lewandowska U, Szewczyk K, Owczarek K, Hrabec Z, Podsędek A, Sosnowska D, et al. Procyanidins from evening primrose (Oenothera paradoxa) defatted seeds inhibit invasiveness of breast cancer cells and modulate the expression of selected genes involved in angiogenesis, metastasis, and apoptosis. Nutr Cancer. 2013;65(8):1219–31. https://​doi.​org/​10.​1080/​01635581.​2013.​830314.CrossRefPubMed
45.
Zurück zum Zitat Richardson MA, Sanders T, Palmer JL, Greisinger A, Singletary SE. Complementary/alternative medicine use in a comprehensive cancer center and the implications for oncology. J Clin Oncol. 2000;18(13):2505–14.CrossRefPubMed Richardson MA, Sanders T, Palmer JL, Greisinger A, Singletary SE. Complementary/alternative medicine use in a comprehensive cancer center and the implications for oncology. J Clin Oncol. 2000;18(13):2505–14.CrossRefPubMed
47.
Zurück zum Zitat Astin J, Reilly C, Perkins C, Child W. Breast cancer patients’ perspectives on and use of complementary and alternative medicine: a study by the Susan G. Komen Breast Cancer Foundation. J Soc Integr Oncol. 2006;4(4):157–69.CrossRefPubMed Astin J, Reilly C, Perkins C, Child W. Breast cancer patients’ perspectives on and use of complementary and alternative medicine: a study by the Susan G. Komen Breast Cancer Foundation. J Soc Integr Oncol. 2006;4(4):157–69.CrossRefPubMed
48.
49.
Zurück zum Zitat Simon O, Vahjen W, Scharek L. Micro-organisms as feed additives-probiotics. Advances in pork Production. 2005;16:161–7. Simon O, Vahjen W, Scharek L. Micro-organisms as feed additives-probiotics. Advances in pork Production. 2005;16:161–7.
56.
Zurück zum Zitat Jakubczyk E, Kosikowska M. Nowa generacja mlecznych produktow fermentowanych z udzialem probiotykow i prebiotykow, produkty synbiotyczne. Prz. Mlecz. 2000;12:397–400. Jakubczyk E, Kosikowska M. Nowa generacja mlecznych produktow fermentowanych z udzialem probiotykow i prebiotykow, produkty synbiotyczne. Prz. Mlecz. 2000;12:397–400.
68.
Zurück zum Zitat Guillot J. Probiotic feed additives. J Vet Pharmacol Ther. 2003;26:52–5. Guillot J. Probiotic feed additives. J Vet Pharmacol Ther. 2003;26:52–5.
70.
Zurück zum Zitat Brandão RL, Castro IM, Bambirra EA, Amaral SC, Fietto LG, Tropia MJM, et al. Intracellular signal triggered by cholera toxin in Saccharomyces boulardii and Saccharomyces cerevisiae. Appl Environ Microbiol. 1998;64(2):564–8.CrossRefPubMedPubMedCentral Brandão RL, Castro IM, Bambirra EA, Amaral SC, Fietto LG, Tropia MJM, et al. Intracellular signal triggered by cholera toxin in Saccharomyces boulardii and Saccharomyces cerevisiae. Appl Environ Microbiol. 1998;64(2):564–8.CrossRefPubMedPubMedCentral
73.
Zurück zum Zitat Matsuzaki T, Yokokura T, Mutai M. The role of lymph node cells in the inhibition of metastasis by subcutaneous injection of Lactobacillus casei in mice. Med Microbiol Immunol. 1988;177(5):245–53.CrossRefPubMed Matsuzaki T, Yokokura T, Mutai M. The role of lymph node cells in the inhibition of metastasis by subcutaneous injection of Lactobacillus casei in mice. Med Microbiol Immunol. 1988;177(5):245–53.CrossRefPubMed
86.
Zurück zum Zitat Urbancsek H, Kazar T, Mezes I, Neumann K. Results of a double-blind, randomized study to evaluate the efficacy and safety of Antibiophilus® in patients with radiation-induced diarrhoea. Eur J Gastroenterol Hepatol. 2001;13(4):391–6.CrossRefPubMed Urbancsek H, Kazar T, Mezes I, Neumann K. Results of a double-blind, randomized study to evaluate the efficacy and safety of Antibiophilus® in patients with radiation-induced diarrhoea. Eur J Gastroenterol Hepatol. 2001;13(4):391–6.CrossRefPubMed
93.
Zurück zum Zitat Bellm L, Epstein J, Rose-Ped A, Martin P, Fuchs H. Patient reports of complications of bone marrow transplantation. Support Care Cancer. 2000;8(1):33–9.CrossRefPubMed Bellm L, Epstein J, Rose-Ped A, Martin P, Fuchs H. Patient reports of complications of bone marrow transplantation. Support Care Cancer. 2000;8(1):33–9.CrossRefPubMed
97.
Zurück zum Zitat Touchefeu Y, Montassier E, Nieman K, Gastinne T, Potel G, Bruley d, et al. Systematic review: the role of the gut microbiota in chemotherapy-or radiation-induced gastrointestinal mucositis–current evidence and potential clinical applications. Aliment Pharmacol Ther. 2014;40(5):409–21. https://doi.org/10.1111/apt.12878.CrossRefPubMed Touchefeu Y, Montassier E, Nieman K, Gastinne T, Potel G, Bruley d, et al. Systematic review: the role of the gut microbiota in chemotherapy-or radiation-induced gastrointestinal mucositis–current evidence and potential clinical applications. Aliment Pharmacol Ther. 2014;40(5):409–21. https://​doi.​org/​10.​1111/​apt.​12878.CrossRefPubMed
100.
Zurück zum Zitat Tijerina AJ. The biochemical basis of metabolism in cancer cachexia. Dimens Crit Care Nurs. 2004;23(6):237–43.CrossRefPubMed Tijerina AJ. The biochemical basis of metabolism in cancer cachexia. Dimens Crit Care Nurs. 2004;23(6):237–43.CrossRefPubMed
125.
Zurück zum Zitat Schagen SB, van Dam FS, Muller MJ, Boogerd W, Lindeboom J, Bruning PF. Cognitive deficits after postoperative adjuvant chemotherapy for breast carcinoma. Cancer. 1999;85(3):640–50.CrossRefPubMed Schagen SB, van Dam FS, Muller MJ, Boogerd W, Lindeboom J, Bruning PF. Cognitive deficits after postoperative adjuvant chemotherapy for breast carcinoma. Cancer. 1999;85(3):640–50.CrossRefPubMed
127.
Zurück zum Zitat Van Dam FS, Boogerd W, Schagen SB, Muller MJ, Droogleever Fortuyn ME, Ev W, et al. Impairment of cognitive function in women receiving adjuvant treatment for high-risk breast cancer: high-dose versus standard-dose chemotherapy. J Natl Cancer Inst. 1998;90(3):210–8.CrossRefPubMed Van Dam FS, Boogerd W, Schagen SB, Muller MJ, Droogleever Fortuyn ME, Ev W, et al. Impairment of cognitive function in women receiving adjuvant treatment for high-risk breast cancer: high-dose versus standard-dose chemotherapy. J Natl Cancer Inst. 1998;90(3):210–8.CrossRefPubMed
128.
Zurück zum Zitat Olin JJ. Cognitive function after systemic therapy for breast cancer. Oncology (Williston Park). 2001;15(5):613–8 discussion 8, 21-4. Olin JJ. Cognitive function after systemic therapy for breast cancer. Oncology (Williston Park). 2001;15(5):613–8 discussion 8, 21-4.
129.
Zurück zum Zitat Pasacreta JV. Depressive phenomena, physical symptom distress, and functional status among women with breast cancer. Nurs Res. 1997;46(4):214–21.CrossRefPubMed Pasacreta JV. Depressive phenomena, physical symptom distress, and functional status among women with breast cancer. Nurs Res. 1997;46(4):214–21.CrossRefPubMed
137.
Zurück zum Zitat Bower JE, Ganz PA, Aziz N, Fahey JL. Fatigue and proinflammatory cytokine activity in breast cancer survivors. Psychosom Med. 2002;64(4):604–11.CrossRefPubMed Bower JE, Ganz PA, Aziz N, Fahey JL. Fatigue and proinflammatory cytokine activity in breast cancer survivors. Psychosom Med. 2002;64(4):604–11.CrossRefPubMed
138.
Zurück zum Zitat Berger AM, Higginbotham P. Correlates of fatigue during and following adjuvant breast cancer chemotherapy: a pilot study. Oncol Nurs Forum. 2000;27(9):1443–8.PubMed Berger AM, Higginbotham P. Correlates of fatigue during and following adjuvant breast cancer chemotherapy: a pilot study. Oncol Nurs Forum. 2000;27(9):1443–8.PubMed
142.
Zurück zum Zitat Samadani AA, Norollahi SE, Rashidy-Pour A, Mansour-Ghanaei F, Nemati S, Joukar F, et al. Cancer signaling pathways with a therapeutic approach; an overview in epigenetic regulation of cancer stem cells. Biomed Pharmacother. 2018;108:590–9.CrossRefPubMed Samadani AA, Norollahi SE, Rashidy-Pour A, Mansour-Ghanaei F, Nemati S, Joukar F, et al. Cancer signaling pathways with a therapeutic approach; an overview in epigenetic regulation of cancer stem cells. Biomed Pharmacother. 2018;108:590–9.CrossRefPubMed
143.
Zurück zum Zitat Samadani AA, Mansour-Ghanaei F, Noroollahi SE. Fluctuations of epigenetic regulation in human gastric adenocarcinoma: how does it affect? Biomed Pharmacother. January 2019;109:144–56.CrossRefPubMed Samadani AA, Mansour-Ghanaei F, Noroollahi SE. Fluctuations of epigenetic regulation in human gastric adenocarcinoma: how does it affect? Biomed Pharmacother. January 2019;109:144–56.CrossRefPubMed
144.
Zurück zum Zitat Akbar Samadani A, Nikbakhsh N, Pilehchian M, Fattahi S, Akhavan-Niaki H. Epigenetic changes of CDX2 in gastric adenocarcinoma. J Cell Commun Signal. 2016. 10(4):267-272. Akbar Samadani A, Nikbakhsh N, Pilehchian M, Fattahi S, Akhavan-Niaki H. Epigenetic changes of CDX2 in gastric adenocarcinoma. J Cell Commun Signal. 2016. 10(4):267-272.
147.
Zurück zum Zitat Kosari-Monfared M, Nikbakhsh N, Fattahi S, Ghadami E, Ranaei M. Hassan Taheri,Fatemeh Amjadi-Moheb,Gholam Ali Godazandeh,Shahryar Shafaei,Maryam Pilehchian Langroudi,Ali Akbar SamadaniHaleh Akhavan-Niaki, CTNNBIP1 downregulation is associated with tumor grade and viral infections in gastric adenocarcinoma. J Cell Physiol. 2018. Kosari-Monfared M, Nikbakhsh N, Fattahi S, Ghadami E, Ranaei M. Hassan Taheri,Fatemeh Amjadi-Moheb,Gholam Ali Godazandeh,Shahryar Shafaei,Maryam Pilehchian Langroudi,Ali Akbar SamadaniHaleh Akhavan-Niaki, CTNNBIP1 downregulation is associated with tumor grade and viral infections in gastric adenocarcinoma. J Cell Physiol. 2018.
148.
Zurück zum Zitat Ghadami E, Nikbakhsh N, Fattahi S, Monfared MK, Ranaee M, Taheri H, et al. Epigenetic alterations of CYLD promoter modulate its expression in gastric adenocarcinoma: a footprint of infections. J Cell Physiol. 2018. https://doi.org/10.1002/jcp.27220. Ghadami E, Nikbakhsh N, Fattahi S, Monfared MK, Ranaee M, Taheri H, et al. Epigenetic alterations of CYLD promoter modulate its expression in gastric adenocarcinoma: a footprint of infections. J Cell Physiol. 2018. https://​doi.​org/​10.​1002/​jcp.​27220.
153.
163.
176.
Zurück zum Zitat Esbona K, Inman D, Saha S, Jeffery J, Schedin P, Wilke L, et al. COX-2 modulates mammary tumor pro77. Lin XB, Farhangfar A, Valcheva R, Sawyer MB, Dieleman L, Schieber A, et al. The role of intestinal microbiota in development of irinotecan toxicity and in toxicity reduction through dietary fibres in rats. PLoS One. 2014;9(1):e83644. https://doi.org/10.1371/journal.pone.0083644.CrossRef Esbona K, Inman D, Saha S, Jeffery J, Schedin P, Wilke L, et al. COX-2 modulates mammary tumor pro77. Lin XB, Farhangfar A, Valcheva R, Sawyer MB, Dieleman L, Schieber A, et al. The role of intestinal microbiota in development of irinotecan toxicity and in toxicity reduction through dietary fibres in rats. PLoS One. 2014;9(1):e83644. https://​doi.​org/​10.​1371/​journal.​pone.​0083644.CrossRef
179.
Zurück zum Zitat Gupta E, Lestingi TM, Mick R, Ramirez J, Vokes EE, Ratain MJ. Metabolic fate of irinotecan in humans: correlation of glucuronidation with diarrhea. Cancer Res. 1994;54(14):3723–5.PubMed Gupta E, Lestingi TM, Mick R, Ramirez J, Vokes EE, Ratain MJ. Metabolic fate of irinotecan in humans: correlation of glucuronidation with diarrhea. Cancer Res. 1994;54(14):3723–5.PubMed
180.
182.
Zurück zum Zitat van Vliet MJ, Tissing WJ, Dun CA, Meessen NE, Kamps WA, de Bont ES, et al. Chemotherapy treatment in pediatric patients with acute myeloid leukemia receiving antimicrobial prophylaxis leads to a relative increase of colonization with potentially pathogenic bacteria in the gut. Clin Infect Dis. 2009;49(2):262–70. https://doi.org/10.1086/599346.CrossRefPubMed van Vliet MJ, Tissing WJ, Dun CA, Meessen NE, Kamps WA, de Bont ES, et al. Chemotherapy treatment in pediatric patients with acute myeloid leukemia receiving antimicrobial prophylaxis leads to a relative increase of colonization with potentially pathogenic bacteria in the gut. Clin Infect Dis. 2009;49(2):262–70. https://​doi.​org/​10.​1086/​599346.CrossRefPubMed
Metadaten
Titel
Gut Microbiota as a Positive Potential Therapeutic Factor in Carcinogenesis: an Overview of Microbiota-Targeted Therapy
Publikationsdatum
26.04.2019
Erschienen in
Journal of Gastrointestinal Cancer / Ausgabe 2/2020
Print ISSN: 1941-6628
Elektronische ISSN: 1941-6636
DOI
https://doi.org/10.1007/s12029-019-00237-6

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