Target intelligence / Profile preview

RAD52 motif containing 1 (RDM1)

Target
RDM1
Molecular classification
DNA repair protein, RNA-binding protein, Homologous recombination factor, Other
01

Overview

RAD52 motif containing 1 (RDM1) is a multifunctional DNA repair protein that contains a motif homologous to the N-terminal region of RAD52, as well as an RNA recognition motif that is absent in RAD52[3]. RDM1 is involved in cellular responses to DNA-damaging agents, especially cisplatin. It plays a pivotal role in DNA double-strand break repair and homologous recombination by binding both single- and double-stranded DNA, especially at sites of genotoxic stress[1][3][5]. RDM1 is frequently overexpressed in several cancers (notably non-small cell lung cancer and breast, ovarian, osteosarcomas) and promotes tumor cell proliferation by supporting cell cycle transitions, suppressing apoptosis, and facilitating signaling pathways such as Raf/ERK and MEK/ERK[3]. It negatively regulates p53 and is proposed to drive oncogenesis and chemoresistance. Knockdown of RDM1 in cancer cell lines increases sensitivity to platinum-based chemotherapeutic agents and enhances apoptosis, supporting its candidacy as both a biomarker and potential therapeutic target in oncology[1][5].

Other names
RAD52 motif-containing protein 1RAD52BMGC33977RAD52 homolog BRAD52 motif 1
02

Mechanism of action

Increased RDM1 expression reduces sensitivity to platinum-based drugs (such as cisplatin) by promoting DNA repair; inhibition sensitizes cells to cisplatin by impeding DNA damage repair; influences cell cycle and apoptosis pathways[1][5]

03

Biological functions

DNA double-strand break repairHomologous recombinationCellular response to cisplatin/genotoxic stressCell cycle regulationNegative regulation of p53Cell proliferationApoptosis suppression
04

Disease associations

CancerChemoresistanceOncogenesisOther
05

Safety considerations

Potential resistance mechanisms and compensatory DNA repairinhibition may increase genomic instability in normal cellsfunctional redundancy with other repair proteins could limit efficacy or affect safety[1][5]
06

Interacting drugs

Cisplatin (primary evidence with regard to chemosensitivity)

1 more in the full profile.

07

Biomarkers

Overexpression correlates with aggressive tumor features and poor prognosis in non-small cell lung cancerproposed as a molecular marker of lung cancer for patient selection[1][5]

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