The role of hypoxia-inducible factor-1 alpha in multidrug-resistant breast cancer
Breast cancer is the most common cancer in women worldwide with increasing incidence. Significant therapeutics advances in the field of breast cancer have resulted in a growing number of treatment options, whereas de novo or acquired resistance is still a persistent clinical challenge. Drug resistan...
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Published in: | Frontiers in oncology Vol. 12; p. 964934 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Frontiers Media S.A
08-08-2022
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Subjects: | |
Online Access: | Get full text |
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Summary: | Breast cancer is the most common cancer in women worldwide with increasing incidence. Significant therapeutics advances in the field of breast cancer have resulted in a growing number of treatment options, whereas
de novo
or acquired resistance is still a persistent clinical challenge. Drug resistance involves a variety of mechanisms, and hypoxia is one of the many causes. Hypoxia-inducible Factor-1 Alpha (HIF-1α) is a key transcription factor which can regulate the response of cells to hypoxia. HIF-1α can trigger anaerobic glycolysis of tumor cells, induce angiogenesis, promote the proliferation, invasion, and migration of tumor cells, and lead to multidrug resistance. This review mainly discusses the role of HIF-1α in the drug-resistant breast cancer and highlighted the potential of HIF-1α -targeted therapy. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 These authors have contributed equally to this work This article was submitted to Pharmacology of Anti-Cancer Drugs, a section of the journal Frontiers in Oncology Reviewed by: Mayank Kumar, University of Florida, United States; Ruby Sharma, Albert Einstein College of Medicine, United States These authors have contributed equally to this work and share last authorship Edited by: Subhadeep Roy, Indian Institute of Technology Delhi, India |
ISSN: | 2234-943X 2234-943X |
DOI: | 10.3389/fonc.2022.964934 |