MicroRNA-21-mediated regulation of Sprouty2 protein expression enhances the cytotoxic effect of 5-fluorouracil and metformin in colon cancer cells

Yin Hsun Feng, Chao-Liang Wu, Ai-Li Shiau, Jenq-Chang Lee, Jan Gowth Chang, Pei-Jung Lu, Chao Ling Tung, Li Yia Feng, Wen Tsung Huang, Chao Jung Tsao

Research output: Contribution to journalArticle

43 Citations (Scopus)

Abstract

Sprouty2 (Spry2) was identified recently as a tumor suppressor gene in cancer cells which inhibits the activation of receptor tyrosine kinases (RTKs). The present study explored the effect of Spry2 in colon cancer cells in order to assess its potential use in the treatment of colon cancer. Expression of Spry2 inhibited the growth of a colon cancer cell line, HCT116, and induced sensitization to fluorouracil (5-FU) and metformin. Spry2 promoted apoptosis of cancer cells in association with activation of the phosphatase and tensin homolog deleted on chromosome 10 (PTEN) pathway and the blockade of Ras-Raf-Erk signaling. Treatment of Spry2-HCT116 cells with metformin resulted in a more prominent effect on the inhibition of cell migration. Inhibition of microRNA-21 (mir-21) induced upregulation of Spry2 and PTEN which underscores the importance of mir-21 in Spry2-associated tumorigenesis of the colon. These results point toward a potential strategy for colon cancer treatment worthy of further investigation.

Original languageEnglish
Pages (from-to)920-926
Number of pages7
JournalInternational journal of molecular medicine
Volume29
Issue number5
DOIs
Publication statusPublished - 2012 May 1

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Metformin
MicroRNAs
Fluorouracil
Colonic Neoplasms
Proteins
Cell Migration Inhibition
HCT116 Cells
Chromosomes, Human, Pair 10
Receptor Protein-Tyrosine Kinases
Tumor Suppressor Genes
Phosphoric Monoester Hydrolases
Neoplasms
Colon
Carcinogenesis
Up-Regulation
Apoptosis
Cell Line
Growth

All Science Journal Classification (ASJC) codes

  • Genetics

Cite this

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abstract = "Sprouty2 (Spry2) was identified recently as a tumor suppressor gene in cancer cells which inhibits the activation of receptor tyrosine kinases (RTKs). The present study explored the effect of Spry2 in colon cancer cells in order to assess its potential use in the treatment of colon cancer. Expression of Spry2 inhibited the growth of a colon cancer cell line, HCT116, and induced sensitization to fluorouracil (5-FU) and metformin. Spry2 promoted apoptosis of cancer cells in association with activation of the phosphatase and tensin homolog deleted on chromosome 10 (PTEN) pathway and the blockade of Ras-Raf-Erk signaling. Treatment of Spry2-HCT116 cells with metformin resulted in a more prominent effect on the inhibition of cell migration. Inhibition of microRNA-21 (mir-21) induced upregulation of Spry2 and PTEN which underscores the importance of mir-21 in Spry2-associated tumorigenesis of the colon. These results point toward a potential strategy for colon cancer treatment worthy of further investigation.",
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MicroRNA-21-mediated regulation of Sprouty2 protein expression enhances the cytotoxic effect of 5-fluorouracil and metformin in colon cancer cells. / Feng, Yin Hsun; Wu, Chao-Liang; Shiau, Ai-Li; Lee, Jenq-Chang; Chang, Jan Gowth; Lu, Pei-Jung; Tung, Chao Ling; Feng, Li Yia; Huang, Wen Tsung; Tsao, Chao Jung.

In: International journal of molecular medicine, Vol. 29, No. 5, 01.05.2012, p. 920-926.

Research output: Contribution to journalArticle

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AU - Lee, Jenq-Chang

AU - Chang, Jan Gowth

AU - Lu, Pei-Jung

AU - Tung, Chao Ling

AU - Feng, Li Yia

AU - Huang, Wen Tsung

AU - Tsao, Chao Jung

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