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Targeting CD82/KAI1 for Precision Therapeutics in Surmounting Metastatic Potential in Breast Cancer

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2021 Sep 10
PMID 34503296
Citations 5
Authors
Affiliations
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Abstract

Metastasis is the main cause of mortality in breast cancer patients. There is an unmet need to develop therapies that can impede metastatic spread. Precision oncology has shown great promise for the treatment of cancers, as the therapeutic approach is tailored to a specific group of patients who are likely to benefit from the treatment, rather than the traditional approach of "one size fits all". CD82, also known as KAI1, a glycoprotein belonging to the tetraspanin family and an established metastasis suppressor, could potentially be exploited to hinder metastases in breast cancer. This review explores the prospect of targeting CD82 as an innovative therapeutic approach in precision medicine for breast cancer patients, with the goal of preventing cancer progression and metastasis. Such an approach would entail the selection of a subset of breast cancer patients with low levels of CD82, and instituting an appropriate treatment scheme tailored towards restoring the levels of CD82 in this group of patients. Proposed precision treatment regimens include current modalities of treating breast cancer, in combination with either clinically approved drugs that could restore the levels of CD82, CD82 peptide mimics or non-coding RNA-based therapeutics.

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References
1.
Forterre A, Komuro H, Aminova S, Harada M . A Comprehensive Review of Cancer MicroRNA Therapeutic Delivery Strategies. Cancers (Basel). 2020; 12(7). PMC: 7408939. DOI: 10.3390/cancers12071852. View

2.
Macfarlane L, Murphy P . MicroRNA: Biogenesis, Function and Role in Cancer. Curr Genomics. 2011; 11(7):537-61. PMC: 3048316. DOI: 10.2174/138920210793175895. View

3.
Guo X, Friess H, Graber H, Kashiwagi M, Zimmermann A, Korc M . KAI1 expression is up-regulated in early pancreatic cancer and decreased in the presence of metastases. Cancer Res. 1996; 56(21):4876-80. View

4.
He B, Liu L, Cook G, Grgurevich S, Jennings L, Zhang X . Tetraspanin CD82 attenuates cellular morphogenesis through down-regulating integrin alpha6-mediated cell adhesion. J Biol Chem. 2004; 280(5):3346-54. DOI: 10.1074/jbc.M406680200. View

5.
Vignoli A, Risi E, McCartney A, Migliaccio I, Moretti E, Malorni L . Precision Oncology via NMR-Based Metabolomics: A Review on Breast Cancer. Int J Mol Sci. 2021; 22(9). PMC: 8124948. DOI: 10.3390/ijms22094687. View