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Allied J Med Res 2017

Volume 1 Issue 2

Herbal Medicine 2017

September 01-02, 2017 London, UK

3

rd

International Conference and Expo on

Herbal & Alternative Medicine

Notes:

Page 38

Korean Scutellaria Georgi flavonoid extract

induces mitochondrially mediated apoptosis

in human gastric cancer AGS cells

Gon Sup Kim

1

, Venu Venkatarame Gowda Saralamma

1

, Ho Jeong

Lee

1

, Gyeong Eun Hong

1

, Hyeon Soo Park

1

, Silvia Yumnam

1

,

Suchismita Raha

1

, Won Sup Lee

2

, Eun Hee Kim

3

, Nak Ju Sung

1

,

Sang Joon Lee

4

and Jeong Doo Heo

4

1

Research Institute of Life science and College of Veterinary Medicine,

Gyeongsang National University, Gazwa, Jinju, Republic of Korea,

2

College of Medicine, Gyeongsang National University, Chilam, Jinju,

Republic of Korea,

3

Department of Nursing Science, International University of Korea,

Jinju, Republic of Korea,

4

Gyeongnam Department of Environment Toxicology and Chemistry,

Gyeongnam Biological Resource Research Center, Korea Institute of

Toxicology, Jinju, Republic of Korea

Objective/Purpose:

In the present study, the anticancer

effect of flavonoid extract from Korean S. baicalensis

Georgi (FSB) was investigated with the aim of elucidating

the underlying molecular mechanisms of the anticancer

effect of FSB on AGS human gastric cancer cells.

Materials & Methods:

The flavonoid compounds were

extracted with 70% methanol from radix of Korean

Scutellaria bicalensis

Georgi (Jinju, Korea). We got the

AGS cells from the Korea Cell Line Bank (Seoul, Korea). All

experiments used that AGS cells were seeded into 6-well

plates and stabilized for 24 h. The cells were then treated

with or without

Scutellaria bicalensis

. Cells were cultured

in RPMI1640 medium supplemented with 10% FBS, and

1% penicillin, streptomycin in a humidified atmosphere

of 5% CO2 at 37°C. Cell viability was determined using

MTT assay. Apoptotic cells were detected using a FITC

annexin-V apoptosis detection kit 1 (BD Pharmingen, San

Diego, CA, USA). And the levels of the apoptosis related

proteins expression were analyzed by Western blot.

Results:

Treatment of AGS cells with FSB significantly

inhibited cell viability in a concentration‑dependent

manner. Furthermore, FSB significantly increased the

proportion of cells in sub‑G1 phase, and Annexin V

and Hoechst 33258 fluorescent staining confirmed the

apoptotic cell death. Furthermore, Western blotting

results identified that treatment of AGS cells with FSB

significantly downregulated the expression of caspase

family members, namely procaspases 3 and 9, and poly

(ADP‑ribose) polymerase (PARP), and subsequently

upregulated cleaved caspase 3 and cleaved PARP. It

was observed that FSB treatment significantly decreased

the mitochondrial membrane potential of AGS cells.

In addition, the ratio of the mitochondrion‑associated

proteins B cell lymphoma 2‑associated X protein and B

cell lymphoma extra-large was upregulated.

Conclusion & Discussion:

The results of the present

study indicate that FSB significantly inhibits cell viability

and induces apoptosis in AGS cells via the mitochondrially

mediated intrinsic apoptotic signalling pathway.

FSB‑induced apoptosis was identified to be mediated

by caspase activation and triggered by the modulation

of Bcl‑2 family proteins. To the best of our knowledge,

the present study is the first to elucidate the underlying

molecular mechanism for the anticancer activity of FSB in

human gastric cancer AGS cells. Therefore, the present

study provides novel insights into the biological effects

of FSB, which may possess therapeutic potential for the

treatment of human gastric cancer.

Biography

Gon Sup Kim has completed his PhD from Seoul National University and

Postdoctoral Studies from University of Pennsylvania School of Veterinary

Medicine. He is the Director of Korea National Animal Bio-resources Bank,

Research Institute of Life Science and Professor of College of Veterinary

Medicine, Gyeongsang National University South Korea.

gons6027@hanmail.net

Gon Sup Kim et al., Allied J Med Res 2017