Literature DB >> 15756446

Establishment and gene analysis of a cisplatin-resistant cell line, Sa-3R, derived from oral squamous cell carcinoma.

Ken Nakatani1, Megumi Nakamura, Katsuhiro Uzawa, Takeshi Wada, Naohiko Seki, Hideki Tanzawa, Shigeyuki Fujita.   

Abstract

Cisplatin (CDDP) is widely used for chemotherapy of many malignancies, especially of oral squamous cell carcinoma (SCC). However, because the mechanism of resistance to CDDP is unclear, we established a CDDP-resistant cell line, Sa-3R, from a CDDP-sensitive cell line, Sa-3, which was derived from moderately differentiated SCC of the lower gingiva. The 3-(3,4-dimethyl-thiazol-2-yl) 2,5-diphenyltetrazolium bromide assay indicated that Sa-3R has 7.5-fold greater resistance to CDDP than Sa-3. Comparing gene expression levels in the cell lines using an in-house cDNA microarray, which represented 2,201 oral disease origin genes, many differentially expressed genes were identified. The ATP-binding cassette transporter genes (MDR-1, MRP-1, and MRP-2), and FANCONI, GRP58, FLJ12089, and SPINT-2 were up-regulated, whereas FOSL1, MRPS27, and PGK-1 were down-regulated. These results were confirmed by semiquantitative reverse transcriptase-polymerase chain reaction. The Sa-3/Sa-3R cell lines could be useful to identify the candidates responsible for the mechanism of CDDP-resistance and the up- or down-regulated genes identified by the gene expression profiles in the Sa-3R cell line may be, in part, associated with the mechanism.

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Year:  2005        PMID: 15756446

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  7 in total

1.  Genes and proteins differentially expressed during in vitro malignant transformation of bovine pancreatic duct cells.

Authors:  R Jesnowski; Dmitri Zubakov; Ralf Faissner; Jörg Ringel; Jörg D Hoheisel; Ralf Lösel; Martina Schnölzer; Matthias Löhr
Journal:  Neoplasia       Date:  2007-02       Impact factor: 5.715

2.  Expression of caveolin-1 and its correlation with cisplatin sensitivity in oral squamous cell carcinoma.

Authors:  Ken Nakatani; Takeshi Wada; Megumi Nakamura; Katsuhiro Uzawa; Hideki Tanzawa; Shigeyuki Fujita
Journal:  J Cancer Res Clin Oncol       Date:  2005-04-26       Impact factor: 4.553

3.  The anti-tumour agent, cisplatin, and its clinically ineffective isomer, transplatin, produce unique gene expression profiles in human cells.

Authors:  Anne M Galea; Vincent Murray
Journal:  Cancer Inform       Date:  2008-06-10

4.  Establishment and characterization of two 5-fluorouracil-resistant hepatocellular carcinoma cell lines.

Authors:  Kazuya Uchibori; Atsushi Kasamatsu; Masahiko Sunaga; Satoshi Yokota; Tomoya Sakurada; Eriko Kobayashi; Masaharu Yoshikawa; Katsuhiro Uzawa; Shiro Ueda; Hideki Tanzawa; Nobunori Sato
Journal:  Int J Oncol       Date:  2011-12-15       Impact factor: 5.650

5.  Identification of genes associated with cisplatin resistance in human oral squamous cell carcinoma cell line.

Authors:  Ping Zhang; Zhiyuan Zhang; Xiaojian Zhou; Weiliu Qiu; Fangan Chen; Wantao Chen
Journal:  BMC Cancer       Date:  2006-09-15       Impact factor: 4.430

6.  EGFR inhibitor enhances cisplatin sensitivity of oral squamous cell carcinoma cell lines.

Authors:  Yukihiro Hiraishi; Takeshi Wada; Ken Nakatani; Itaru Tojyo; Takashi Matsumoto; Norifumi Kiga; Kenji Negoro; Shigeyuki Fujita
Journal:  Pathol Oncol Res       Date:  2008-03-07       Impact factor: 3.201

7.  Potential implications of GRP58 expression and susceptibility of cervical cancer to cisplatin and thymoquinone-based therapy.

Authors:  Wan Abd Ghani Wan Nor Hafiza; Saiful Yazan Latifah
Journal:  Onco Targets Ther       Date:  2014-08-07       Impact factor: 4.147

  7 in total

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