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Page 58

Volume 3

August 5-6, 2019 | Singapore

CANCER RESEARCH AND PHARMACOLOGY

STRUCTURAL BIOCHEMISTRY, STEM CELLS AND MOLECULAR BIOLOGY

24

th

International Conference on

International Congress on

&

Cancer Research 2019 & Structural Biochemistry 2019

August 5-6, 2019

Journal of Cancer and Metastasis Research

Clin Psychol Cog Sci, Volume 3

Does the PARP inhibitor Olaparib increase anti-tumor activity of the BET inhibitor JQ1

in invasive lobular carcinoma cells?

Elisha Eshkour

RCSI, Ireland

I

nvasive lobular carcinoma (ILC) is the second most common sub-type of breast cancer, compromising 10% of all cases.

BET inhibitors represent a novel class of anticancer agents that are clinically relevant in the treatment of ILC, however, their

efficacy as single agents are limited. Recent studies demonstrate increased anti-tumour activity of BET inhibitors with the

addition of a PARP inhibitor. The aim of this project was to investigate the effects of combining the BET inhibitor, JQ1, with the

PARP inhibitor Olaparib, in an

in vitro

model of ILC. Molecular characterization via western blotting identified the CAMA-1

and OCUB-M cell lines as appropriate models of ILC. Initial IC50 characterization experiments completed using the MTT assay

demonstrated CAMA-1 cells were more resistant to JQ1 inhibition. Subsequent analysis of the expression of BCL2, an anti-

apoptotic gene, was carried out in both cell line models, with the CAMA1 cells demonstrating higher expression of this gene,

suggesting an intrinsic resistance to cell death. Synergy assays performed revealed synergistic effects of combination treatment

JQ1 and Olaparib. This was further shown through enhanced PARP cleavage seen in the CAMA1 cells, suggesting sensitization

of CAMA1 cells to JQ1 induced death with the addition of Olaparib. In OCUB-M cells, PARP cleavage was not affected by the

addition of Olaparib to JQ1. The results observed in the CAMA1 cells demonstrate the potential of sensitizing BRCA proficient

cells to treatment with PARP inhibition, and the use of a combination therapy for anti-cancer treatment.

elisha.eshkour@gmail.com