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Cyclin C: A new responser for chemosensitivity in cancer
The resistance to cisplatin‐based chemotherapy is a common cause of poor prognosis in cancer patients. Cisplatin stimulation causes cyclin C translocating to mitochondria, and in turn induces mitochondrial fission. However, little is known about the role of cyclin C in mitochondrial dysfunction in c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042672/ https://www.ncbi.nlm.nih.gov/pubmed/35475325 http://dx.doi.org/10.1002/ctm2.833 |
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author | Fang, Shuai Jin, Xiaofeng Zhou, Chengwei Gong, Zhaohui |
author_facet | Fang, Shuai Jin, Xiaofeng Zhou, Chengwei Gong, Zhaohui |
author_sort | Fang, Shuai |
collection | PubMed |
description | The resistance to cisplatin‐based chemotherapy is a common cause of poor prognosis in cancer patients. Cisplatin stimulation causes cyclin C translocating to mitochondria, and in turn induces mitochondrial fission. However, little is known about the role of cyclin C in mitochondrial dysfunction in cancer cells challenged with cisplatin. In the present commentary, we bring to the attention of readers the recent report by Jiang et al which revealed the importance of ubiquitylation and translocation of cyclin C in gastric cancer cells in response to cisplatin stimulation for mitochondrial stability. This finding provides new insights into exploring the novel mechanisms of chemoresistance and developing the new chemotherapy synergistic agents in the era of precision oncology. |
format | Online Article Text |
id | pubmed-9042672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90426722022-04-28 Cyclin C: A new responser for chemosensitivity in cancer Fang, Shuai Jin, Xiaofeng Zhou, Chengwei Gong, Zhaohui Clin Transl Med Commentary The resistance to cisplatin‐based chemotherapy is a common cause of poor prognosis in cancer patients. Cisplatin stimulation causes cyclin C translocating to mitochondria, and in turn induces mitochondrial fission. However, little is known about the role of cyclin C in mitochondrial dysfunction in cancer cells challenged with cisplatin. In the present commentary, we bring to the attention of readers the recent report by Jiang et al which revealed the importance of ubiquitylation and translocation of cyclin C in gastric cancer cells in response to cisplatin stimulation for mitochondrial stability. This finding provides new insights into exploring the novel mechanisms of chemoresistance and developing the new chemotherapy synergistic agents in the era of precision oncology. John Wiley and Sons Inc. 2022-04-26 /pmc/articles/PMC9042672/ /pubmed/35475325 http://dx.doi.org/10.1002/ctm2.833 Text en © 2022 The Authors. Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Commentary Fang, Shuai Jin, Xiaofeng Zhou, Chengwei Gong, Zhaohui Cyclin C: A new responser for chemosensitivity in cancer |
title | Cyclin C: A new responser for chemosensitivity in cancer |
title_full | Cyclin C: A new responser for chemosensitivity in cancer |
title_fullStr | Cyclin C: A new responser for chemosensitivity in cancer |
title_full_unstemmed | Cyclin C: A new responser for chemosensitivity in cancer |
title_short | Cyclin C: A new responser for chemosensitivity in cancer |
title_sort | cyclin c: a new responser for chemosensitivity in cancer |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042672/ https://www.ncbi.nlm.nih.gov/pubmed/35475325 http://dx.doi.org/10.1002/ctm2.833 |
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