Previous Page  11 / 12 Next Page
Information
Show Menu
Previous Page 11 / 12 Next Page
Page Background

Page 35

Notes:

conferenceseries

.com

Volume 2, Issue 2 (Suppl)

Breast Can Curr Res

ISSN: 2572-4118 BCCR, an open access journal

Breast Cancer Summit 2017

May 08-10, 2017

May 08-10, 2017 Singapore

4

th

World Congress on

Breast Cancer

Thymoquinone inhibits bone metastasis of triple negative breast cancer cells through the suppression of

CXCR4 signaling axis

Muthu K Shanmugam, Annie Hsu, Gautam Sethi and Benny K H Tan

National University of Singapore, Singapore

S

everal lines of evidence(s) indicate that CXCR4 overexpression has been correlated with distant site metastasis and poor overall

survival rate in patient with breast cancer. The tumor metastasis promoting molecule CXCR4 is considered as a potential therapeutic

target for inhibiting breast cancer metastasis. Thus, novel agents that can down-regulate CXCR4 expression have potential against breast

cancer metastasis. In the present report we investigated the effect of thymoquinone (TQ), derived from the seeds of medicinal plant

Nigella sativa

, on the expression and regulation of CXCR4 in breast cancer cells. In addition, we evaluated the effect of TQ in a metastasis

mouse model established by intracardiac injection of luciferase-tagged MDA-MB-231 breast cancer cells that metastasize to the bones.

We observed that TQ could inhibit the expression of CXCR4 in MCF-7 and MDA-MB-231 cells in a dose and time dependent manner.

TQ (2 mg/kg or 4 mg/kg) treatment for four weeks significantly inhibited tumor growth and significantly reduced metastases to multiple

vital organs, including lungs, brain and bone. Immuno-histochemical analysis of the lung and brain tissue showed significant reduction

in the expression of CXCR4, Ki67, MMP9, VEGFR2 and COX2 compared to tissues from control mice. TQ treatment also reduced

the overall bone tumor burden. Overall, our results show that TQ exerts its antitumor and anti-metastatic effects by downregulation of

CXCR4 expression both

in vitro

and

in vivo

thus may have possible potential for the treatment of breast cancer.

Acknowledgement:

This work was supported by NUHS Basic Seed Research grant to Prof. Benny Tan.

Biography

Muthu K Shanmugam is a senior research fellow in the Department of Pharmacology, National University of Singapore, Yong Loo Lin School of Medicine. He got his

Ph.D in cancer pharmacology and he is currently working as a senior research fellow. He has twelve years of experience in experimental laboratory research and

have published in journal papers and presented at international conferences. Muthu K Shanmugam has vast experience in cancer biology, inflammatory diseases,

orthotopic, xenograft and transgenic mice models, in molecular biology, cell and tissue culture experiments. In addition, he is trained in high-throughput technology

such as cDNA microarray technology, antigen and antibody array technology, two dimensional gel electrophoresis, mass spectrometry, pharmacokinetics and in

the development of array based clinical diagnostic tools.

phcsmk@nus.edu.sg

Muthu K Shanmugam et al., Breast Can Curr Res 2017, 2:2(Suppl)

http://dx.doi.org/10.4172/2572-4118-C1-002