Phenotypic mismatch repair hMSH2 and hMLH1 gene expression profiles in primary non-small cell lung carcinomas

作者：Vageli Dimitra^*; Daniil Zoe; Dahabreh Jubrail; Karagianni Eleni; Vamvakopoulou Dimitra N; Ioannou Maria G; Scarpinato Karin; Vamvakopoulos Nikos C; Gourgoulianis Konstantinos I; Koukoulis George K

来源：Lung Cancer, 2009, 64(3): 282-288.

DOI：10.1016/j.lungcan.2008.09.018

• MMR
• hMSH2
• hMLH1
• Q-RT-PCR
• NSCLC
• Phenotype

Background: Defects in the human DNA mismatch repair genes (MMR) hMSH2 and hMLH1 arc responsible for the development of sporadic and hereditary colorectal cancers. The role of MMR genes in the pathogenesis of lung cancer has not been elucidated. The aim of this study was to address the phenotypic mRNA expression profiles of mismatch DNA repair system in lung cancer.
Materials and methods: We evaluated the mRNA levels of the hMSH2 and hMLH1 components of the mismatch DNA repair (MMR) system in 29 unselected frozen pairs of primary non-small cell lung carcinomas (NSCLCs) and their adjacent normal tissue (ANTs) specimens by quantitative real-time PCR analysis relative to housekeeping Porphobilinogen deaminase (hPBGD) mRNA. To simplify and potentially improve the analysis of data, we defined for each individual MMR mRNA two possible phenotypes: a regular (R(2): hMSH2/hPBGD mRNAs >= 1 and R(1): hMLH1/hPBGD mRNAs >= 1) and a reduced (r(2): hMSH2/hPBGD mRNAs < 1 and r(1): hMLH1/hPBGD mRNAs < 1). The presence of MMR gene expression was evaluated after conversion of the molecular mRNA levels into clinically distinct phenotypic entities by these working criteria, based on the hypothesis that reduced mRNA and protein levels result in lower or non-functional MMR.
Results: Phenotyping defined four distinct MMR system expression profiles, R(2)R(1), r(2)R(1), R(2)r(1) and r(2)r(1) by ascending tumor progression rate and identified a previously unrecognized disease-associated phenotypic entity (r(2)r(1)). The phenotype-based biological aspects of the MMR system suggested that its two components: (1) function independently and (2) are not directly involved in the onset of the transformation process, since healthy lung tissue was devoid of r(2)r(1) phenotypes.
Conclusion: These findings link MMR mRNA levels of paired lung tissue specimens to patients' clinical condition and suggest that phenotypic translation of molecular MMR data refines the biology of the MMR system with consequent diagnostic implications in the clinical assessment of lung cancer patients.

• 出版日期2009-6