Drug intelligence / Profile preview

MAL-5

Development stage
Preclinical
Lead developer
University of Sharjah
Modality
Small Molecules
Administration
Parenteral
01

Overview

MAL-5 is an experimental small molecule histone deacetylase (HDAC) inhibitor being investigated as a potential anti-metastatic therapy for breast cancer. Developed by researchers at the University of Sharjah and the University of Freiburg, MAL-5 has demonstrated preclinical efficacy in inhibiting the growth and invasion of breast cancer cell lines, including MCF-7 and MDA-MB-231. Mechanistically, treatment with MAL-5 significantly induces the expression of tissue inhibitor of metalloproteinases 2 (TIMP-2) at both the mRNA and protein levels, while simultaneously reducing the expression and enzymatic activity of matrix metalloproteinase-2 (MMP-2) and matrix metalloproteinase-9 (MMP-9). This modulation of the TIMP/MMP signaling pathway effectively attenuates the invasive and metastatic capabilities of breast cancer cells.

02

Targets

HDAC (HDAC family)TIMP2MMP2 (Matrix metalloproteinase-2)MMP9 (Matrix metalloproteinase-9)

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