Literature DB >> 21036757

TS, DHFR and GARFT expression in non-squamous cell carcinoma of NSCLC and malignant pleural mesothelioma patients treated with pemetrexed.

Hidetaka Uramoto1, Takamitsu Onitsuka, Hidehiko Shimokawa, Takeshi Hanagiri.   

Abstract

BACKGROUND: Recently, pemetrexed (PEM), a new generation antifolate, has been used for the treatment of patients with advanced non-squamous cell carcinoma (SQ) of non-small cell lung cancer (NSCLC) and malignant pleural mesothelioma (MPM). However, no useful markers for selecting appropriate candidates exist at present.
MATERIALS AND METHODS: Tumor specimens were collected from 5 lung non-SQ and 8 MPM patients who underwent surgery and received PEM. Real-time PCR and immunohistochemical (IHC) staining of the primary tumor were used to analyze the mRNA and protein expressions of thymidylate synthase (TS)/dihydrofolate reductase (DHFR), and glycinamide ribonucleotide formyltransferase (GARFT), and to compare the expression status and clinical outcomes.
RESULTS: TS, DHFR, and GARFT mRNA levels had a median value of 2.39, 1.70, and 1.40 in non-SQ samples of NSCLC patients. The TS and DHFR protein levels had a mean total score of 2 and 4 in non-SQ of NSCLC patients. TS, DHFR, and GARFT mRNA levels had a median value of 5.55, 3.73, and 3.52 in MPM patients. TS and DHFR protein levels had a mean total expression score of 1 and 3 in MPM patients. No significant correlation was identified between the expression levels of TS/DPD/GARFT mRNA and clinical response for the non-SQ of NSCLC and MPM patients treated with PEM.
CONCLUSION: TS, DHFR, and GARFT mRNA and protein expression may not be useful markers for predicting clinical response in Japanese patients with non-SQ of NSCLC and MPM. Further investigations are necessary in order to develop biomarkers to determine the clinical benefits of PEM treatment.

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Year:  2010        PMID: 21036757

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  5 in total

1.  Thymidylate synthase as a determinant of pemetrexed sensitivity in non-small cell lung cancer.

Authors:  K Takezawa; I Okamoto; W Okamoto; M Takeda; K Sakai; S Tsukioka; K Kuwata; H Yamaguchi; K Nishio; K Nakagawa
Journal:  Br J Cancer       Date:  2011-04-12       Impact factor: 7.640

2.  Plasma thymidylate synthase and dihydrofolate reductase mRNA levels as potential predictive biomarkers of pemetrexed sensitivity in patients with advanced non-small cell lung cancer.

Authors:  Tao Li; Jin-Bo Huang; Jun-Guo Lu; Rong Li; Yan Wang; Xiang-Rong Shi; Min-Xin Shi; Xiao-Dong Zhang
Journal:  J Thorac Dis       Date:  2020-12       Impact factor: 2.895

3.  Successful first-line treatment of simultaneous multiple primary malignancies of lung adenocarcinoma and renal clear cell carcinoma: A case report.

Authors:  Xiaojun Ye; Xiangliang Liu; Na Yin; Wei Song; Jin Lu; Yi Yang; Xiao Chen
Journal:  Front Immunol       Date:  2022-08-01       Impact factor: 8.786

4.  Pharmacogenomic assessment of outcomes of pemetrexed-treated patients with adenocarcinoma of the lung.

Authors:  Minkyu Jung; Chul Ho Lee; Hyung Soon Park; Ji Hyun Lee; Young Ae Kang; Se Kyu Kim; Joon Chang; Dae Joon Kim; Sun Young Rha; Joo Hang Kim; Byoung Chul Cho
Journal:  Yonsei Med J       Date:  2013-07       Impact factor: 2.759

Review 5.  The pemetrexed-containing treatments in the non-small cell lung cancer is -/low thymidylate synthase expression better than +/high thymidylate synthase expression: a meta-analysis.

Authors:  Lei Wang; Rui Wang; Yunjian Pan; Yihua Sun; Jie Zhang; Haiquan Chen
Journal:  BMC Cancer       Date:  2014-03-19       Impact factor: 4.430

  5 in total

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