Helveticoside Exhibited p53-dependent Anticancer Activity Against Colorectal Cancer
Na An
1
,
Ying Sun
2
,
Ligang Ma
1
,
Sheng-Li Shi
1
,
Xiaoke Zheng
3
,
Weisheng Feng
3
,
Zhiming Shan
4
,
Yongguang Han
1
,
Le Zhao
1
,
Huiming Wu
1
Publication type: Journal Article
Publication date: 2020-04-01
scimago Q1
wos Q2
SJR: 1.029
CiteScore: 8.9
Impact factor: 3.4
ISSN: 01884409, 18735487
PubMed ID:
32147288
General Medicine
Abstract
Investigation into the anti-cancer activities of natural products and their derivatives represents an efficient approach to develop safe and effective chemotherapeutic agents for the treatment of colorectal cancer. Helveticoside is a biologically active component of the seed extract of Descurainia sophia. This compound has been reported to regulate the genes related to cell proliferation and apoptosis in lung cancer cells, however its anticancer activity has not been fully explored yet.Cell viability was evaluated by MTT and Trypan blue exclusion assay; cell apoptosis was measured by flow cytometry; mitochondrial membrane potential was determined by using JC1-mitochondrial membrane potential assay kit; protein levels were determined by western blot assay; in vivo tumor growth was assessed in a xenograft nude mice model.The current study demonstrated the in vitro anti-cancer activity of helveticoside against colorectal cancer using colorectal cancer cells SW480 and HCT116. Moreover, induction of apoptosis was found to mediate the cytotoxic action of helveticoside on SW480 and HCT116 cells. Based on the decrease in the mitochondrial membrane potential, upregulation of Bax, downregulation of Bcl-2 and cleavage of caspase-3 and 9, apoptosis was induced by helveticoside via mitochondria-mediated intrinsic apoptotic signaling pathways in colorectal cancer cells. Besides, using p53-knockout SW480 cells, the cytotoxic action of helveticoside was found to be p53-dependent. More importantly, administration of helveticoside inhibited the growth of HCT116 cells derived-colorectal cancer xenograft in mice via activation of apoptosis.Helveticoside might be a potential candidate for the development of novel chemotherapeutic agents for the treatment of colorectal cancer, while the potential toxic effects of helveticoside may be worthy of further investigations.
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Total citations:
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Citations from 2024:
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(44.44%)
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MLA
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GOST
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An N. et al. Helveticoside Exhibited p53-dependent Anticancer Activity Against Colorectal Cancer // Archives of Medical Research. 2020. Vol. 51. No. 3. pp. 224-232.
GOST all authors (up to 50)
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An N., Sun Y., Ma L., Shi S., Zheng X., Feng W., Shan Z., Han Y., Zhao L., Wu H. Helveticoside Exhibited p53-dependent Anticancer Activity Against Colorectal Cancer // Archives of Medical Research. 2020. Vol. 51. No. 3. pp. 224-232.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1016/j.arcmed.2020.02.007
UR - https://doi.org/10.1016/j.arcmed.2020.02.007
TI - Helveticoside Exhibited p53-dependent Anticancer Activity Against Colorectal Cancer
T2 - Archives of Medical Research
AU - An, Na
AU - Sun, Ying
AU - Ma, Ligang
AU - Shi, Sheng-Li
AU - Zheng, Xiaoke
AU - Feng, Weisheng
AU - Shan, Zhiming
AU - Han, Yongguang
AU - Zhao, Le
AU - Wu, Huiming
PY - 2020
DA - 2020/04/01
PB - Elsevier
SP - 224-232
IS - 3
VL - 51
PMID - 32147288
SN - 0188-4409
SN - 1873-5487
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2020_An,
author = {Na An and Ying Sun and Ligang Ma and Sheng-Li Shi and Xiaoke Zheng and Weisheng Feng and Zhiming Shan and Yongguang Han and Le Zhao and Huiming Wu},
title = {Helveticoside Exhibited p53-dependent Anticancer Activity Against Colorectal Cancer},
journal = {Archives of Medical Research},
year = {2020},
volume = {51},
publisher = {Elsevier},
month = {apr},
url = {https://doi.org/10.1016/j.arcmed.2020.02.007},
number = {3},
pages = {224--232},
doi = {10.1016/j.arcmed.2020.02.007}
}
Cite this
MLA
Copy
An, Na, et al. “Helveticoside Exhibited p53-dependent Anticancer Activity Against Colorectal Cancer.” Archives of Medical Research, vol. 51, no. 3, Apr. 2020, pp. 224-232. https://doi.org/10.1016/j.arcmed.2020.02.007.