β‑glucan vaccine adjuvant approach for cancer treatment through immune enhancement (B‑VACCIEN) in specific immunocompromised populations (Review)
The incidence of cancer, which is the second leading cause of mortality globally, continues to increase, although continued efforts are being made to identify effective treatments with fewer side‑effects. Previous studies have reported that chronic microinflammation, which occurs in diseases, includ...
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Published in | Oncology reports Vol. 47; no. 1 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Spandidos Publications UK Ltd
01.01.2022
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Abstract | The incidence of cancer, which is the second leading cause of mortality globally, continues to increase, although continued efforts are being made to identify effective treatments with fewer side‑effects. Previous studies have reported that chronic microinflammation, which occurs in diseases, including diabetes, along with weakened immune systems, may ultimately lead to cancer development. Chemotherapy, radiotherapy and surgery are the mainstream approaches to treatment; however, they all lead to immune system weakness, which in turn increases the metastatic spread. The aim of the present review was to provide evidence of a biological response modifier β‑glucan [β‑glucan vaccine adjuvant approach to treating cancer via immune enhancement (B‑VACCIEN)] and its beneficial effects, including vaccine‑adjuvant potential, balancing metabolic parameters (including blood glucose and lipid levels), increasing peripheral blood cell cytotoxicity against cancer and alleviating chemotherapy side effects in animal models. This suggests its value as a potential strategy to provide long‑term prophylaxis in immunocompromised individuals or genetically prone to cancer. |
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AbstractList | The incidence of cancer, which is the second leading cause of mortality globally, continues to increase, although continued efforts are being made to identify effective treatments with fewer side‑effects. Previous studies have reported that chronic microinflammation, which occurs in diseases, including diabetes, along with weakened immune systems, may ultimately lead to cancer development. Chemotherapy, radiotherapy and surgery are the mainstream approaches to treatment; however, they all lead to immune system weakness, which in turn increases the metastatic spread. The aim of the present review was to provide evidence of a biological response modifier β‑glucan [β‑glucan vaccine adjuvant approach to treating cancer via immune enhancement (B‑VACCIEN)] and its beneficial effects, including vaccine‑adjuvant potential, balancing metabolic parameters (including blood glucose and lipid levels), increasing peripheral blood cell cytotoxicity against cancer and alleviating chemotherapy side effects in animal models. This suggests its value as a potential strategy to provide long‑term prophylaxis in immunocompromised individuals or genetically prone to cancer. The incidence of cancer, which is the second leading cause of mortality globally, continues to increase, although continued efforts are being made to identify effective treatments with fewer side‑effects. Previous studies have reported that chronic microinflammation, which occurs in diseases, including diabetes, along with weakened immune systems, may ultimately lead to cancer development. Chemotherapy, radiotherapy and surgery are the mainstream approaches to treatment; however, they all lead to immune system weakness, which in turn increases the metastatic spread. The aim of the present review was to provide evidence of a biological response modifier β‑glucan [β‑glucan vaccine adjuvant approach to treating cancer via immune enhancement (B‑VACCIEN)] and its beneficial effects, including vaccine‑adjuvant potential, balancing metabolic parameters (including blood glucose and lipid levels), increasing peripheral blood cell cytotoxicity against cancer and alleviating chemotherapy side effects in animal models. This suggests its value as a potential strategy to provide long‑term prophylaxis in immunocompromised individuals or genetically prone to cancer.The incidence of cancer, which is the second leading cause of mortality globally, continues to increase, although continued efforts are being made to identify effective treatments with fewer side‑effects. Previous studies have reported that chronic microinflammation, which occurs in diseases, including diabetes, along with weakened immune systems, may ultimately lead to cancer development. Chemotherapy, radiotherapy and surgery are the mainstream approaches to treatment; however, they all lead to immune system weakness, which in turn increases the metastatic spread. The aim of the present review was to provide evidence of a biological response modifier β‑glucan [β‑glucan vaccine adjuvant approach to treating cancer via immune enhancement (B‑VACCIEN)] and its beneficial effects, including vaccine‑adjuvant potential, balancing metabolic parameters (including blood glucose and lipid levels), increasing peripheral blood cell cytotoxicity against cancer and alleviating chemotherapy side effects in animal models. This suggests its value as a potential strategy to provide long‑term prophylaxis in immunocompromised individuals or genetically prone to cancer. |
ArticleNumber | 14 |
Author | Kisaka, Tomohiko Kumar, Seydunganallu Kurosawa, Gene Senthilkumar, Rajappa Srinivasan, Subramaniam Osawa, Hiroshi Iwasaki, Masaru Rao, Kosagi-Sharaf Dedeepiya, Vidyasagar Abraham, Samuel Ikewaki, Nobunao Vaddi, Suryaprakash Raghavan, Kadalraja Preethy, Senthilkumar |
Author_xml | – sequence: 1 givenname: Nobunao surname: Ikewaki fullname: Ikewaki, Nobunao organization: Department of Medical Life Science, Kyushu University of Health and Welfare, Nobeoka, Miyazaki 882‑8508, Japan – sequence: 2 givenname: Vidyasagar surname: Dedeepiya fullname: Dedeepiya, Vidyasagar organization: The Mary‑Yoshio Translational Hexagon (MYTH), Nichi‑In Centre for Regenerative Medicine (NCRM), Chennai 600034, India – sequence: 3 givenname: Kadalraja surname: Raghavan fullname: Raghavan, Kadalraja organization: Department of Paediatric Neurology, Kenmax Medical Service Private Limited, Tallakulam, Madurai 625002, India – sequence: 4 givenname: Kosagi-Sharaf surname: Rao fullname: Rao, Kosagi-Sharaf organization: Institute of Scientific Research and High Technology Services of Panama (INDICASAT‑AIP), Clayton 88888, Republic of Panama – sequence: 5 givenname: Suryaprakash surname: Vaddi fullname: Vaddi, Suryaprakash organization: Department of Urology, Yashoda Hospitals, Hyderabad, Telangana 50008, India – sequence: 6 givenname: Hiroshi surname: Osawa fullname: Osawa, Hiroshi organization: Clinical Services Department, Omote Medical Clinic, Chiba 296‑8602, Japan – sequence: 7 givenname: Tomohiko surname: Kisaka fullname: Kisaka, Tomohiko organization: Division of Biodesign, Office of Research and Academic‑Government‑Community Collaboration, Hiroshima University, Higashihiroshima, Hiroshima 739‑8511, Japan – sequence: 8 givenname: Gene surname: Kurosawa fullname: Kurosawa, Gene organization: Department of Academic Research Support Promotion Facility, Center for Research Promotion and Support, Fujita Health University, Toyoake, Aichi 470‑1192, Japan – sequence: 9 givenname: Subramaniam surname: Srinivasan fullname: Srinivasan, Subramaniam organization: The Mary‑Yoshio Translational Hexagon (MYTH), Nichi‑In Centre for Regenerative Medicine (NCRM), Chennai 600034, India – sequence: 10 givenname: Seydunganallu surname: Kumar fullname: Kumar, Seydunganallu organization: Department of Sociology, Manonmaniyam Sundaranar University, Abishekapatti, Tamil Nadu 627012, India – sequence: 11 givenname: Rajappa surname: Senthilkumar fullname: Senthilkumar, Rajappa organization: The Fujio‑Eiji Academic Terrain (FEAT), Nichi‑In Centre for Regenerative Medicine (NCRM), Chennai 600034, India – sequence: 12 givenname: Masaru surname: Iwasaki fullname: Iwasaki, Masaru organization: Centre for Advancing Clinical Research (CACR), University of Yamanashi‑ School of Medicine, Chuo, Yamanashi 409‑3898, Japan – sequence: 13 givenname: Senthilkumar surname: Preethy fullname: Preethy, Senthilkumar organization: The Fujio‑Eiji Academic Terrain (FEAT), Nichi‑In Centre for Regenerative Medicine (NCRM), Chennai 600034, India – sequence: 14 givenname: Samuel surname: Abraham fullname: Abraham, Samuel organization: The Mary‑Yoshio Translational Hexagon (MYTH), Nichi‑In Centre for Regenerative Medicine (NCRM), Chennai 600034, India |
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SubjectTerms | Adjuvants, Vaccine - administration & dosage Aging Animals Antigens beta-Glucans - immunology Cancer therapies Chemotherapy Cytotoxicity Diabetes Disease prevention DNA damage Health risk assessment Humans Hyperglycemia Hypothalamus Immune system Immunocompromised Host - immunology Inflammation Metabolic disorders Mortality Neoplasms - immunology Neoplasms - prevention & control Older people Phytochemicals Prostate cancer Radiation therapy Surgery Vaccines |
Title | β‑glucan vaccine adjuvant approach for cancer treatment through immune enhancement (B‑VACCIEN) in specific immunocompromised populations (Review) |
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