File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Decoding CLU (Clusterin): Conquering cancer treatment resistance and immunological barriers

TitleDecoding CLU (Clusterin): Conquering cancer treatment resistance and immunological barriers
Authors
KeywordsClusterin
Immunosuppression
Therapy resistance
Issue Date20-Aug-2024
PublisherElsevier
Citation
International Immunopharmacology, 2024, v. 137 How to Cite?
Abstract

One major obstacle in the treatment of cancer is the presence of proteins resistant to cancer therapy, which can impede the effectiveness of traditional approaches such as radiation and chemotherapy. This resistance can lead to disease progression and cause treatment failure. Extensive research is currently focused on studying these proteins to create tailored treatments that can circumvent resistance mechanisms. CLU (Clusterin), a chaperone protein, has gained notoriety for its role in promoting resistance to a wide range of cancer treatments, including chemotherapy, radiation therapy, and targeted therapy. The protein has also been discovered to have a role in regulating the immunosuppressive environment within tumors. Its ability to influence oncogenic signaling and inhibit cell death bolster cancer cells resistant against treatments, which poses a significant challenge in the field of oncology. Researchers are actively investigating to the mechanisms by which CLU exerts its resistance-promoting effects, with the ultimate goal of developing strategies to circumvent its impact and enhance the effectiveness of cancer therapies. By exploring CLU's impact on cancer, resistance mechanisms, tumor microenvironment (TME), and therapeutic strategies, this review aims to contribute to the ongoing efforts to improve cancer treatment outcomes.


Persistent Identifierhttp://hdl.handle.net/10722/358458
ISSN
2023 Impact Factor: 4.8
2023 SCImago Journal Rankings: 1.167

 

DC FieldValueLanguage
dc.contributor.authorMamun, M. A.A.-
dc.contributor.authorZheng, Yi Chao-
dc.contributor.authorWang, Ning-
dc.contributor.authorWang, Bo-
dc.contributor.authorZhang, Yu-
dc.contributor.authorPang, Jing Ru-
dc.contributor.authorShen, Dan Dan-
dc.contributor.authorLiu, Hong Min-
dc.contributor.authorGao, Ya-
dc.date.accessioned2025-08-07T00:32:27Z-
dc.date.available2025-08-07T00:32:27Z-
dc.date.issued2024-08-20-
dc.identifier.citationInternational Immunopharmacology, 2024, v. 137-
dc.identifier.issn1567-5769-
dc.identifier.urihttp://hdl.handle.net/10722/358458-
dc.description.abstract<p>One major obstacle in the treatment of cancer is the presence of proteins resistant to cancer therapy, which can impede the effectiveness of traditional approaches such as radiation and chemotherapy. This resistance can lead to disease progression and cause treatment failure. Extensive research is currently focused on studying these proteins to create tailored treatments that can circumvent resistance mechanisms. CLU (Clusterin), a chaperone protein, has gained notoriety for its role in promoting resistance to a wide range of cancer treatments, including chemotherapy, radiation therapy, and targeted therapy. The protein has also been discovered to have a role in regulating the immunosuppressive environment within tumors. Its ability to influence oncogenic signaling and inhibit cell death bolster cancer cells resistant against treatments, which poses a significant challenge in the field of oncology. Researchers are actively investigating to the mechanisms by which CLU exerts its resistance-promoting effects, with the ultimate goal of developing strategies to circumvent its impact and enhance the effectiveness of cancer therapies. By exploring CLU's impact on cancer, resistance mechanisms, tumor microenvironment (TME), and therapeutic strategies, this review aims to contribute to the ongoing efforts to improve cancer treatment outcomes.</p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofInternational Immunopharmacology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectClusterin-
dc.subjectImmunosuppression-
dc.subjectTherapy resistance-
dc.titleDecoding CLU (Clusterin): Conquering cancer treatment resistance and immunological barriers-
dc.typeArticle-
dc.identifier.doi10.1016/j.intimp.2024.112355-
dc.identifier.pmid38851158-
dc.identifier.scopuseid_2-s2.0-85195423479-
dc.identifier.volume137-
dc.identifier.eissn1878-1705-
dc.identifier.issnl1567-5769-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats