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REG I enhances chemo‐ and radiosensitivity in squamous cell esophageal cancer cells

Identification of reliable markers of chemo‐ and radiosensitivity and the key molecules that enhance the susceptibility of squamous esophageal cancer cells to anticancer treatments would be highly desirable. To test whether regenerating gene (REG) I expression enhances chemo‐ and radiosensitivity in...

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Published in:Cancer science 2008-12, Vol.99 (12), p.2491-2495
Main Authors: Hayashi, Kaori, Motoyama, Satoru, Koyota, Souichi, Koizumi, Yukio, Wang, Jingshu, Takasawa, Shin, Itaya‐Hironaka, Asako, Sakuramoto‐Tsuchida, Sumiyo, Maruyama, Kiyotomi, Saito, Hajime, Minamiya, Yoshihiro, Ogawa, Jun‐ichi, Sugiyama, Toshihiro
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container_title Cancer science
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creator Hayashi, Kaori
Motoyama, Satoru
Koyota, Souichi
Koizumi, Yukio
Wang, Jingshu
Takasawa, Shin
Itaya‐Hironaka, Asako
Sakuramoto‐Tsuchida, Sumiyo
Maruyama, Kiyotomi
Saito, Hajime
Minamiya, Yoshihiro
Ogawa, Jun‐ichi
Sugiyama, Toshihiro
description Identification of reliable markers of chemo‐ and radiosensitivity and the key molecules that enhance the susceptibility of squamous esophageal cancer cells to anticancer treatments would be highly desirable. To test whether regenerating gene (REG) I expression enhances chemo‐ and radiosensitivity in esophageal squamous cell carcinoma cells, we used MTT (3‐[4,5‐dimethylthiazol‐2‐yl]‐2,5‐diphenyltetrazolium bromide) assays to compare the chemo‐ and radiosensitivities of untransfected TE‐5 and TE‐9 cells with those of cells stably transfected with REG Iα and Iβ. We then used flow cytometry to determine whether REG I expression alters cell cycle progression. No REG I mRNA or protein were detected in untransfected TE‐5 and TE‐9 cells. Transfection with REG Iα and Iβ led to strong expression of both REG I mRNA and protein in TE‐5 and TE‐9 cells, which in turn led to significant increases in both chemo‐ and radiosensitivity. Cell cycle progression was unaffected by REG I expression. REG I thus appears to enhance the chemo‐ and radiosensitivity of squamous esophageal cancer cells, which suggests that it may be a useful target for improved and more individualized treatments for patients with esophageal squamous cell carcinoma. (Cancer Sci 2008; 99: 2491–2495)
doi_str_mv 10.1111/j.1349-7006.2008.00980.x
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REG I thus appears to enhance the chemo‐ and radiosensitivity of squamous esophageal cancer cells, which suggests that it may be a useful target for improved and more individualized treatments for patients with esophageal squamous cell carcinoma. 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subjects Antimetabolites, Antineoplastic - metabolism
Antimetabolites, Antineoplastic - therapeutic use
Biological and medical sciences
Carcinoma, Squamous Cell - drug therapy
Carcinoma, Squamous Cell - genetics
Carcinoma, Squamous Cell - metabolism
Carcinoma, Squamous Cell - pathology
Carcinoma, Squamous Cell - radiotherapy
Cell Line, Tumor
Cell Proliferation - drug effects
Cell Proliferation - radiation effects
Dose-Response Relationship, Radiation
Esophageal Neoplasms - drug therapy
Esophageal Neoplasms - genetics
Esophageal Neoplasms - metabolism
Esophageal Neoplasms - pathology
Esophageal Neoplasms - radiotherapy
Fluorouracil - metabolism
Fluorouracil - therapeutic use
Formazans - metabolism
Humans
Lithostathine - genetics
Lithostathine - metabolism
Medical sciences
Original
Proteins - metabolism
Radiation Tolerance - genetics
RNA, Messenger - metabolism
Tetrazolium Salts - metabolism
Transfection
Tumors
title REG I enhances chemo‐ and radiosensitivity in squamous cell esophageal cancer cells
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