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Volume 9, Issue 11 (Suppl)

J Cancer Sci Ther

ISSN: 1948-5956 JCST, an open access journal

Asia Pacific Oncologists 2017

November 20-22, 2017

November 20-22, 2017 Melbourne, Australia

14

th

Asia Pacific

Oncologists Annual Meeting

Differential effects of fatty acid binding protein-7 (FABP7) in triple negative breast cancer cell lines

HS578T and MDA-MB-231 under hypoxic condition

Kwong Soke Chee, Rhodes A, Taib N A and Chung I

University of Malaya, Malaysia

T

riple negative breast cancer (TNBC) is the most aggressive subtype which contributes to approximately 10% of breast

cancer cases. The absence of ER-, PR- and HER2 receptors in TNBC leaves this subtype with no targeted therapy. Recent

studies showed that FABP7 is shown to significantly overexpress in TNBC tissues compared to other subtypes. FABPs are

known to be lipid chaperones and they can affect lipid metabolism. To date, the evidence on its prognostic role in TNBC

is contrasting. Liu et al. (2012) shows that FABP7 expression correlates with lower overall and recurrence-free survival. In

contrast, two other studies by Alshareeda, et al. (2012) and Zhang, et al. (2010) demonstrates that FABP7-positive basal tumors

are associated with better prognosis. Hence, we aim to investigate the function of FABP7 in TNBC through

in vitro

models.

Despite the excessive FABP7 expression in TNBC tissue, FABP7 protein was not detected in TNBC cell lines (HS578T and

MDA-MB-231). However, chronic hypoxia increased FABP7 mRNA expression in these cell lines. It indicates that FABP7

might only be important in hypoxic conditions. As FABP7 was not naturally expressed in the TNBC cell lines used in our study,

we generated FABP7-transduced TNBC cell lines with lentivirus particles. MTT assay showed that FABP7 caused reduced cell

viability in HS578T but not MDA-MB-231 cells under hypoxic condition. This study shows that FABP7 can cause cell death in

HS578T cells under hypoxic condition but not in the more aggressive MDA-MB-231 cells. More research on FABP7 in TNBC

is warranted as it could serve as a potential molecular target for TNBC.

Biography

Kwong Soke Chee is currently a PhD student at University of Malaya, Malaysia. Her research interest includes molecular biology and lipidomics. In specific,

her project focuses on the function of FABP7 in TNBC. Besides doing bench work in the laboratory, she also has experience in recruiting patients for breast

cancer cohort. In year 2015, she was selected to participate in Novartis International Biocamp in Basel, Switzerland to gain insights into research and business

environment in pharmaceutical industry.

sokechee@yahoo.com

Kwong Soke Chee

et.al

., J Cancer Sci Ther 2017, 9:11 (Suppl)

DOI: 10.4172/1948-5956-C1-117