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Targeting TMEM88 as an Attractive Therapeutic Strategy in Malignant Tumors

According to authoritative surveys, the overall morbidity and mortality of malignant tumors show an upward trend, and it is predicted that this trend will not be well contained in the upcoming new period. Since the influencing factors, pathogenesis, and progression characteristics of malignant tumor...

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Autores principales: Cai, Ming, Ni, Wei-Jian, Wang, Ying-Hong, Wang, Jing-Ji, Zhou, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207468/
https://www.ncbi.nlm.nih.gov/pubmed/35734592
http://dx.doi.org/10.3389/fonc.2022.906372
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author Cai, Ming
Ni, Wei-Jian
Wang, Ying-Hong
Wang, Jing-Ji
Zhou, Hong
author_facet Cai, Ming
Ni, Wei-Jian
Wang, Ying-Hong
Wang, Jing-Ji
Zhou, Hong
author_sort Cai, Ming
collection PubMed
description According to authoritative surveys, the overall morbidity and mortality of malignant tumors show an upward trend, and it is predicted that this trend will not be well contained in the upcoming new period. Since the influencing factors, pathogenesis, and progression characteristics of malignant tumors have not been fully elucidated, the existing treatment strategies, mainly including surgical resection, ablation therapy and chemotherapy, cannot achieve satisfactory results. Therefore, exploring potential therapeutic targets and clarifying their functions and mechanisms in continuous research and practice will provide new ideas and possibilities for the treatment of malignant tumors. Recently, a double-transmembrane protein named transmembrane protein 88 (TMEM88) was reported to regulate changes in downstream effectors by mediating different signaling pathways and was confirmed to be widely involved in cell proliferation, differentiation, apoptosis and tumor progression. At present, abnormal changes in TMEM88 have been found in breast cancer, ovarian cancer, lung cancer, thyroid cancer and other malignant tumors, which has also attracted the attention of tumor research and attempted to clarify its function and mechanism. However, due to the lack of systematic generalization, comprehensive and detailed research results have not been comprehensively summarized. In view of this, this article will describe in detail the changes in TMEM88 in the occurrence and development of malignant tumors, comprehensively summarize the corresponding molecular mechanisms, and explore the potential of targeting TMEM88 in the treatment of malignant tumors to provide valuable candidate targets and promising intervention strategies for the diagnosis and cure of malignant tumors.
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spelling pubmed-92074682022-06-21 Targeting TMEM88 as an Attractive Therapeutic Strategy in Malignant Tumors Cai, Ming Ni, Wei-Jian Wang, Ying-Hong Wang, Jing-Ji Zhou, Hong Front Oncol Oncology According to authoritative surveys, the overall morbidity and mortality of malignant tumors show an upward trend, and it is predicted that this trend will not be well contained in the upcoming new period. Since the influencing factors, pathogenesis, and progression characteristics of malignant tumors have not been fully elucidated, the existing treatment strategies, mainly including surgical resection, ablation therapy and chemotherapy, cannot achieve satisfactory results. Therefore, exploring potential therapeutic targets and clarifying their functions and mechanisms in continuous research and practice will provide new ideas and possibilities for the treatment of malignant tumors. Recently, a double-transmembrane protein named transmembrane protein 88 (TMEM88) was reported to regulate changes in downstream effectors by mediating different signaling pathways and was confirmed to be widely involved in cell proliferation, differentiation, apoptosis and tumor progression. At present, abnormal changes in TMEM88 have been found in breast cancer, ovarian cancer, lung cancer, thyroid cancer and other malignant tumors, which has also attracted the attention of tumor research and attempted to clarify its function and mechanism. However, due to the lack of systematic generalization, comprehensive and detailed research results have not been comprehensively summarized. In view of this, this article will describe in detail the changes in TMEM88 in the occurrence and development of malignant tumors, comprehensively summarize the corresponding molecular mechanisms, and explore the potential of targeting TMEM88 in the treatment of malignant tumors to provide valuable candidate targets and promising intervention strategies for the diagnosis and cure of malignant tumors. Frontiers Media S.A. 2022-06-06 /pmc/articles/PMC9207468/ /pubmed/35734592 http://dx.doi.org/10.3389/fonc.2022.906372 Text en Copyright © 2022 Cai, Ni, Wang, Wang and Zhou https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Cai, Ming
Ni, Wei-Jian
Wang, Ying-Hong
Wang, Jing-Ji
Zhou, Hong
Targeting TMEM88 as an Attractive Therapeutic Strategy in Malignant Tumors
title Targeting TMEM88 as an Attractive Therapeutic Strategy in Malignant Tumors
title_full Targeting TMEM88 as an Attractive Therapeutic Strategy in Malignant Tumors
title_fullStr Targeting TMEM88 as an Attractive Therapeutic Strategy in Malignant Tumors
title_full_unstemmed Targeting TMEM88 as an Attractive Therapeutic Strategy in Malignant Tumors
title_short Targeting TMEM88 as an Attractive Therapeutic Strategy in Malignant Tumors
title_sort targeting tmem88 as an attractive therapeutic strategy in malignant tumors
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207468/
https://www.ncbi.nlm.nih.gov/pubmed/35734592
http://dx.doi.org/10.3389/fonc.2022.906372
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