1 H NMR-Based metabolic profiles delineate the anticancer effect of vitamin C and oxaliplatin on hepatocellular carcinoma cells

Hepatocellular carcinoma (HCC) is a leading cause of cancer death worldwide. Because of its high recurrence rate and heterogeneity, effective treatment for advanced stage of HCC is currently lacking. There are accumulating evidences showing the therapeutic potential of pharmacologic vitamin C (VC) o...

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Main Authors: Lin, Caigui, Dong, Jiyang, Wei, Zhiliang, Cheng, Kian-Kai, Li, Jie, You, Song, Liu, Yueyue, Wang, Xiaomin, Chen, Zhong
Format: Article
Published: American Chemical Society 2020
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Online Access:http://eprints.utm.my/id/eprint/87248/
http://dx.doi.org/10.1021/acs.jproteome.9b00635
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Institution: Universiti Teknologi Malaysia
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spelling my.utm.872482020-10-31T12:27:04Z http://eprints.utm.my/id/eprint/87248/ 1 H NMR-Based metabolic profiles delineate the anticancer effect of vitamin C and oxaliplatin on hepatocellular carcinoma cells Lin, Caigui Dong, Jiyang Wei, Zhiliang Cheng, Kian-Kai Li, Jie You, Song Liu, Yueyue Wang, Xiaomin Chen, Zhong TP Chemical technology Hepatocellular carcinoma (HCC) is a leading cause of cancer death worldwide. Because of its high recurrence rate and heterogeneity, effective treatment for advanced stage of HCC is currently lacking. There are accumulating evidences showing the therapeutic potential of pharmacologic vitamin C (VC) on HCC. However, the metabolic basis underlying the anticancer property of VC remains to be elucidated. In this study, we used a high-resolution proton nuclear magnetic resonance-based metabolomics technique to assess the global metabolic changes in HCC cells following VC treatment. In addition, the HCC cells were also treated with oxaliplatin (OXA) to explore the potential synergistic effect induced by the combined VC and OXA treatment. The current metabolomics data suggested different mechanisms of OXA and VC in modulating cell growth and metabolism. In general, VC treatment led to inhibition of energy metabolism via NAD+ depletion and amino acid deprivation. On the other hand, OXA caused significant perturbation in phospholipid biosynthesis and phosphatidylcholine biosynthesis pathways. The current results highlighted glutathione metabolism, and pathways related to succinate and choline may play central roles in conferring the combined effect between OXA and VC. Taken together, this study provided metabolic evidence of VC and OXA in treating HCC and may contribute toward the potential application of combined VC and OXA as complementary HCC therapies. American Chemical Society 2020 Article PeerReviewed Lin, Caigui and Dong, Jiyang and Wei, Zhiliang and Cheng, Kian-Kai and Li, Jie and You, Song and Liu, Yueyue and Wang, Xiaomin and Chen, Zhong (2020) 1 H NMR-Based metabolic profiles delineate the anticancer effect of vitamin C and oxaliplatin on hepatocellular carcinoma cells. Journal of Proteome Research, 19 (2). pp. 781-793. ISSN 1535-3893 http://dx.doi.org/10.1021/acs.jproteome.9b00635
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
topic TP Chemical technology
spellingShingle TP Chemical technology
Lin, Caigui
Dong, Jiyang
Wei, Zhiliang
Cheng, Kian-Kai
Li, Jie
You, Song
Liu, Yueyue
Wang, Xiaomin
Chen, Zhong
1 H NMR-Based metabolic profiles delineate the anticancer effect of vitamin C and oxaliplatin on hepatocellular carcinoma cells
description Hepatocellular carcinoma (HCC) is a leading cause of cancer death worldwide. Because of its high recurrence rate and heterogeneity, effective treatment for advanced stage of HCC is currently lacking. There are accumulating evidences showing the therapeutic potential of pharmacologic vitamin C (VC) on HCC. However, the metabolic basis underlying the anticancer property of VC remains to be elucidated. In this study, we used a high-resolution proton nuclear magnetic resonance-based metabolomics technique to assess the global metabolic changes in HCC cells following VC treatment. In addition, the HCC cells were also treated with oxaliplatin (OXA) to explore the potential synergistic effect induced by the combined VC and OXA treatment. The current metabolomics data suggested different mechanisms of OXA and VC in modulating cell growth and metabolism. In general, VC treatment led to inhibition of energy metabolism via NAD+ depletion and amino acid deprivation. On the other hand, OXA caused significant perturbation in phospholipid biosynthesis and phosphatidylcholine biosynthesis pathways. The current results highlighted glutathione metabolism, and pathways related to succinate and choline may play central roles in conferring the combined effect between OXA and VC. Taken together, this study provided metabolic evidence of VC and OXA in treating HCC and may contribute toward the potential application of combined VC and OXA as complementary HCC therapies.
format Article
author Lin, Caigui
Dong, Jiyang
Wei, Zhiliang
Cheng, Kian-Kai
Li, Jie
You, Song
Liu, Yueyue
Wang, Xiaomin
Chen, Zhong
author_facet Lin, Caigui
Dong, Jiyang
Wei, Zhiliang
Cheng, Kian-Kai
Li, Jie
You, Song
Liu, Yueyue
Wang, Xiaomin
Chen, Zhong
author_sort Lin, Caigui
title 1 H NMR-Based metabolic profiles delineate the anticancer effect of vitamin C and oxaliplatin on hepatocellular carcinoma cells
title_short 1 H NMR-Based metabolic profiles delineate the anticancer effect of vitamin C and oxaliplatin on hepatocellular carcinoma cells
title_full 1 H NMR-Based metabolic profiles delineate the anticancer effect of vitamin C and oxaliplatin on hepatocellular carcinoma cells
title_fullStr 1 H NMR-Based metabolic profiles delineate the anticancer effect of vitamin C and oxaliplatin on hepatocellular carcinoma cells
title_full_unstemmed 1 H NMR-Based metabolic profiles delineate the anticancer effect of vitamin C and oxaliplatin on hepatocellular carcinoma cells
title_sort 1 h nmr-based metabolic profiles delineate the anticancer effect of vitamin c and oxaliplatin on hepatocellular carcinoma cells
publisher American Chemical Society
publishDate 2020
url http://eprints.utm.my/id/eprint/87248/
http://dx.doi.org/10.1021/acs.jproteome.9b00635
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