A H2AX?CARP-1 Interaction Regulates Apoptosis Signaling Following DNA Damage.

ABSTRACT: Cell Cycle and Apoptosis Regulatory Protein (CARP-1/CCAR1) is a peri-nuclear phosphoprotein that regulates apoptosis via chemotherapeutic Adriamycin (doxorubicin) and a novel class of CARP-1 functional mimetic (CFM) compounds. Although Adriamycin causes DNA damage, data from Comet assays revealed that CFM-4.16 also induced DNA damage. Phosphorylation of histone 2AX (?H2AX) protein is involved in regulating DNA damage repair and apoptosis signaling. Adriamycin or CFM-4.16 treatments inhibited cell growth and caused elevated CARP-1 and ?H2AX in human breast (HBC) and cervical cancer (HeLa) cells. In fact, a robust nuclear or peri-nuclear co-localization of CARP-1 and ?H2AX occurred in cells undergoing apoptosis. Knock-down of CARP-1 diminished ?H2AX, their co-localization, and apoptosis in CFM-4.16- or Adriamycin-treated cells. We found that CARP-1 directly binds with H2AX, and H2AX interacted with CARP-1, but not CARP-1 (?600?652) mutant. Moreover, cells expressing CARP-1 (?600?652) mutant were resistant to apoptosis, and had diminished levels of ?H2AX, when compared with cells expressing wild-type CARP-1. Mutagenesis studies revealed that H2AX residues 1?35 harbored a CARP-1-binding epitope, while CARP-1 amino acids 636?650 contained an H2AX-interacting epitope. Surface plasmon resonance studies revealed that CARP-1 (636?650) peptide bound with H2AX (1?35) peptide with a dissociation constant (Kd) of 127 nM. Cells expressing enhanced GFP (EGFP)-tagged H2AX (1?35) peptide or EGFP-tagged CARP-1 (636?650) peptide were resistant to inhibition by Adriamycin or CFM-4.16. Treatment of cells with transactivator of transcription (TAT)-tagged CARP-1 (636?650) peptide resulted in a moderate, statistically significant abrogation of Adriamycin-induced growth inhibition of cancer cells. Our studies provide evidence for requirement of CARP-1 interaction with H2AX in apoptosis signaling by Adriamycin and CFM compounds.

SUBMITTER: Sekhar SC 

PROVIDER: S-EPMC6406907 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature