Role of PDLIM4 and c-Src in breast cancer progression


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Abstract

High heterogeneity is characteristic of oncology diseases, often complicating the choice of optimal anticancer treatment. One cancer type may combine tumors differing in histogenesis, genetic lesions, and mechanism of cell transformation. Differences in the mechanism of cell malignant transformation result in specifics of cancer cell metabolism and sensitivity to various agents, including anticancer treatments. Hence, the molecular subtype of a tumor is essential to know for choosing the optimal therapeutic strategy. The review considers the role actin-associated proteins and tyrosine kinases, in particular, PDLIM4 and Src kinase, play in the formation of pathological signaling pathways.

About the authors

D. S. Kravchenko

Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry; Engelhardt Institute of Molecular Biology

Author for correspondence.
Email: stepan@chumakov.email
Russian Federation, Moscow, 117997; Moscow, 117997

E. I. Frolova

Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry

Email: stepan@chumakov.email
Russian Federation, Moscow, 117997

J. E. Kravchenko

Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry; Engelhardt Institute of Molecular Biology

Email: stepan@chumakov.email
Russian Federation, Moscow, 117997; Moscow, 117997

S. P. Chumakov

Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry; Engelhardt Institute of Molecular Biology

Email: stepan@chumakov.email
Russian Federation, Moscow, 117997; Moscow, 117997

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