Use of aspirin in the prevention of colorectal cancer through TIGIT‐CD155 pathway
Colorectal cancer (CRC) is one of the most widespread malignant cancers, with a high incidence and mortality all over the world. Aspirin (ASA) otherwise known as acetylsalicylic acid, is a non‐steroidal anti‐inflammatory drug that has shown promising results in the prevention of chronic diseases, in...
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Published in | Journal of cellular and molecular medicine Vol. 23; no. 7; pp. 4514 - 4522 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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England
John Wiley & Sons, Inc
01.07.2019
John Wiley and Sons Inc |
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Abstract | Colorectal cancer (CRC) is one of the most widespread malignant cancers, with a high incidence and mortality all over the world. Aspirin (ASA) otherwise known as acetylsalicylic acid, is a non‐steroidal anti‐inflammatory drug that has shown promising results in the prevention of chronic diseases, including several cancers. In previous studies, aspirin has been shown to reduce the incidence of CRC. Immune checkpoint blockade of T cell Ig and ITIM domain receptor (TIGIT) alone or combined with other immune checkpoint blockades moleculars has gained impressive results in the treatment of the melanoma and glioblastoma. Here, we found that TIGIT and Poliovirus receptor (PVR, CD155) are expressed in tumour cells; the TIGIT and CD155 protein expression in cancer tissue has been found to be significantly higher than that in the precancerous tissue. T cell Ig and ITIM domain receptor and CD226 were expressed in the lymphocytes near the tumour tissue and the adjacent tissues. Aspirin has been found to inhibit cancer cell viability and promote CRC cell apoptosis.Similarly, aspirin has also been found to increase pro‐apoptotic protein Bax's expression. We found that the expression of TIGIT decreased with an increase in the concentration of aspirin and that the suppression of TIGIT can affect the effect of aspirin on cell proliferation. In this paper, we found that aspirin attenuates cancer cell proliferation and induces CRC cells apoptosis by down‐regulating the expression of TIGIT, which provides new evidence for the application of aspirin in cancer treatment. |
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AbstractList | Colorectal cancer (CRC) is one of the most widespread malignant cancers, with a high incidence and mortality all over the world. Aspirin (ASA) otherwise known as acetylsalicylic acid, is a non‐steroidal anti‐inflammatory drug that has shown promising results in the prevention of chronic diseases, including several cancers. In previous studies, aspirin has been shown to reduce the incidence of CRC. Immune checkpoint blockade of T cell Ig and ITIM domain receptor (TIGIT) alone or combined with other immune checkpoint blockades moleculars has gained impressive results in the treatment of the melanoma and glioblastoma. Here, we found that TIGIT and Poliovirus receptor (PVR, CD155) are expressed in tumour cells; the TIGIT and CD155 protein expression in cancer tissue has been found to be significantly higher than that in the precancerous tissue. T cell Ig and ITIM domain receptor and CD226 were expressed in the lymphocytes near the tumour tissue and the adjacent tissues. Aspirin has been found to inhibit cancer cell viability and promote CRC cell apoptosis.Similarly, aspirin has also been found to increase pro‐apoptotic protein Bax's expression. We found that the expression of TIGIT decreased with an increase in the concentration of aspirin and that the suppression of TIGIT can affect the effect of aspirin on cell proliferation. In this paper, we found that aspirin attenuates cancer cell proliferation and induces CRC cells apoptosis by down‐regulating the expression of TIGIT, which provides new evidence for the application of aspirin in cancer treatment. Abstract Colorectal cancer (CRC) is one of the most widespread malignant cancers, with a high incidence and mortality all over the world. Aspirin (ASA) otherwise known as acetylsalicylic acid, is a non‐steroidal anti‐inflammatory drug that has shown promising results in the prevention of chronic diseases, including several cancers. In previous studies, aspirin has been shown to reduce the incidence of CRC. Immune checkpoint blockade of T cell Ig and ITIM domain receptor (TIGIT) alone or combined with other immune checkpoint blockades moleculars has gained impressive results in the treatment of the melanoma and glioblastoma. Here, we found that TIGIT and Poliovirus receptor (PVR, CD155) are expressed in tumour cells; the TIGIT and CD155 protein expression in cancer tissue has been found to be significantly higher than that in the precancerous tissue. T cell Ig and ITIM domain receptor and CD226 were expressed in the lymphocytes near the tumour tissue and the adjacent tissues. Aspirin has been found to inhibit cancer cell viability and promote CRC cell apoptosis.Similarly, aspirin has also been found to increase pro‐apoptotic protein Bax's expression. We found that the expression of TIGIT decreased with an increase in the concentration of aspirin and that the suppression of TIGIT can affect the effect of aspirin on cell proliferation. In this paper, we found that aspirin attenuates cancer cell proliferation and induces CRC cells apoptosis by down‐regulating the expression of TIGIT, which provides new evidence for the application of aspirin in cancer treatment. |
Author | Su, Chunxia Zhang, Dong Yang, Shaoqi Zhou, Qiunan Yang, Xiaojuan Duan, Xiangguo Li, Hai Ma, Bin Liu, Juanxi Du, Yong |
AuthorAffiliation | 2 Department of Oncology Surgery The First People's Hospital of Yinchuan Yinchuan China 5 Department of Gastroenterology General Hospital of Ningxia Medical University Yinchuan China 1 Department of Laboratory Medicine College of Clinical Medicine, Ningxia Medical University Yinchuan China 3 Department of Laboratory Surgery General Hospital of Ningxia Medical University Yinchuan China 4 Department of Colorectal Surgery General Hospital of Ningxia Medical University Yinchuan China 6 Department of Pathogen Biology and Immunology, School of Basic Medical Science Ningxia Medical University Yinchuan China |
AuthorAffiliation_xml | – name: 6 Department of Pathogen Biology and Immunology, School of Basic Medical Science Ningxia Medical University Yinchuan China – name: 4 Department of Colorectal Surgery General Hospital of Ningxia Medical University Yinchuan China – name: 2 Department of Oncology Surgery The First People's Hospital of Yinchuan Yinchuan China – name: 3 Department of Laboratory Surgery General Hospital of Ningxia Medical University Yinchuan China – name: 5 Department of Gastroenterology General Hospital of Ningxia Medical University Yinchuan China – name: 1 Department of Laboratory Medicine College of Clinical Medicine, Ningxia Medical University Yinchuan China |
Author_xml | – sequence: 1 givenname: Bin surname: Ma fullname: Ma, Bin organization: The First People's Hospital of Yinchuan – sequence: 2 givenname: Xiangguo surname: Duan fullname: Duan, Xiangguo email: duanxiangguo@nxmu.edu.cn organization: General Hospital of Ningxia Medical University – sequence: 3 givenname: Qiunan orcidid: 0000-0002-9523-1973 surname: Zhou fullname: Zhou, Qiunan organization: College of Clinical Medicine, Ningxia Medical University – sequence: 4 givenname: Juanxi surname: Liu fullname: Liu, Juanxi organization: College of Clinical Medicine, Ningxia Medical University – sequence: 5 givenname: Xiaojuan surname: Yang fullname: Yang, Xiaojuan organization: College of Clinical Medicine, Ningxia Medical University – sequence: 6 givenname: Dong surname: Zhang fullname: Zhang, Dong organization: General Hospital of Ningxia Medical University – sequence: 7 givenname: Shaoqi surname: Yang fullname: Yang, Shaoqi organization: General Hospital of Ningxia Medical University – sequence: 8 givenname: Yong surname: Du fullname: Du, Yong organization: General Hospital of Ningxia Medical University – sequence: 9 givenname: Hai surname: Li fullname: Li, Hai email: zhuoran1126@163.com organization: General Hospital of Ningxia Medical University – sequence: 10 givenname: Chunxia surname: Su fullname: Su, Chunxia email: 1651085195@qq.com organization: Ningxia Medical University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31090213$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_tranon_2021_101062 crossref_primary_10_1038_s41598_024_64447_0 crossref_primary_10_3389_fonc_2022_844260 crossref_primary_10_1038_s41392_020_00348_8 crossref_primary_10_1186_s40364_023_00543_z crossref_primary_10_3389_fimmu_2020_551057 crossref_primary_10_1016_j_semcancer_2020_07_001 crossref_primary_10_2174_1573394718666220930143651 crossref_primary_10_1111_jgh_15730 crossref_primary_10_3390_curroncol30070460 crossref_primary_10_1002_iub_2461 crossref_primary_10_1155_2021_5440572 crossref_primary_10_1186_s12964_020_00638_2 |
Cites_doi | 10.1111/j.1572-0241.2000.03360.x 10.1200/JCO.2015.65.3519 10.1093/annonc/mdi006 10.1016/j.virusres.2017.09.001 10.1073/pnas.97.12.6803 10.1038/sj.cdd.4401733 10.1016/j.bcp.2007.09.020 10.1136/gut.49.2.236 10.1038/ni.1674 10.1093/carcin/bgl071 10.1182/blood-2004-09-3548 10.1007/s00428-006-0338-7 10.1523/JNEUROSCI.0054-18.2018 10.1158/0008-5472.CAN-04-2682 10.1136/bmj.i6188 10.4049/jimmunol.0901226 |
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Copyright | 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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Keywords | aspirin CD226 colorectal cancer cell proliferation TIGIT CD155 |
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License | Attribution 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
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Snippet | Colorectal cancer (CRC) is one of the most widespread malignant cancers, with a high incidence and mortality all over the world. Aspirin (ASA) otherwise known... Abstract Colorectal cancer (CRC) is one of the most widespread malignant cancers, with a high incidence and mortality all over the world. Aspirin (ASA)... |
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SubjectTerms | Acetylsalicylic acid Alcohol Alzheimer's disease Antigens Antigens, Differentiation, T-Lymphocyte - metabolism Apoptosis Apoptosis - drug effects Aspirin Aspirin - pharmacology Aspirin - therapeutic use BAX protein bcl-2-Associated X Protein - metabolism Cancer Cancer therapies CD155 CD155 antigen CD226 Cell adhesion & migration Cell growth Cell Movement - drug effects Cell proliferation Cell Survival - drug effects Cell viability Colorectal cancer Colorectal carcinoma Colorectal Neoplasms - drug therapy Colorectal Neoplasms - pathology Colorectal Neoplasms - prevention & control Disease prevention Flow cytometry Glioblastoma HT29 Cells Humans Immune checkpoint Immune system Immunoglobulins Incidence Inflammation Lymphocytes Lymphocytes - metabolism Lymphocytes T Medical prognosis Medical research Melanoma Original Proteins R&D Receptors, Immunologic - metabolism Receptors, Virus - metabolism Research & development Researchers Signal Transduction - drug effects T cell receptors TIGIT Tissues Tumors |
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Title | Use of aspirin in the prevention of colorectal cancer through TIGIT‐CD155 pathway |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjcmm.14332 https://www.ncbi.nlm.nih.gov/pubmed/31090213 https://www.proquest.com/docview/2247641596 https://search.proquest.com/docview/2232030516 https://pubmed.ncbi.nlm.nih.gov/PMC6584546 |
Volume | 23 |
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