Claudins: The Newly Emerging Targets in Breast Cancer

被引:7
作者
Yadav, Reena [1 ]
Kumar, Yashwant [2 ]
Dahiya, Divya [3 ]
Bhatia, Alka [1 ]
机构
[1] Postgrad Inst Med Educ & Res, Dept Expt Med & Biotechnol, Chandigarh, India
[2] Postgrad Inst Med Educ & Res, Dept Immunopathol, Chandigarh, India
[3] Postgrad Inst Med Educ & Res, Dept Gen Surg, Chandigarh, India
关键词
Chemoresistance; Metastasis; Therapeutics; Tumorigenesis; Tight junctions; TIGHT JUNCTION PROTEINS; BLOOD-BRAIN-BARRIER; INVASIVE DUCTAL CARCINOMA; GROWTH-FACTOR-BETA; OVARIAN-CANCER; TRANSCRIPTION FACTOR; GENE-EXPRESSION; SUBCELLULAR-LOCALIZATION; DIFFERENTIAL EXPRESSION; REDUCED EXPRESSION;
D O I
10.1016/j.clbc.2022.09.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Claudin-low breast cancers are recently described entities showing low expression of certain claudins and cell adhesion molecules. Claudins constitute the backbone of tight junctions (TJs) formed between 2 cells. Their dysregulation plays a vital role in tumorigenesis. First part of the article focuses on the role of claudins in the TJ organization, their structural-functional characteristics, and post-transcriptional and translational modifications. The latter part of the review attempts to summarize existing knowledge regarding the status of claudins in breast cancer. The article also provides an overview of the effect of claudins on tumor progression, metastasis, stemness, chemotherapy resistance, and their crosstalk with relevant signaling pathways in breast cancer. Claudins can act as 2-edged swords in tumors. Some claudins have either tumor-suppressive/ promoting action, while others work as both in a context-dependent manner. Claudins regulate many important events in breast cancer. However, the intricacies involved in their activity are poorly understood. Post-translational modifications in claudins and their impact on TJ integrity, function, and tumor behavior are still unclear. Although their role in adverse events in breast cancer is recognized, their potential to serve as relevant targets for future therapeutics, especially for difficult-to-treat subtypes of the above malignancy, remains to be explored.
引用
收藏
页码:737 / 752
页数:16
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