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Erschienen in: Pathology & Oncology Research 2/2018

22.04.2017 | Original Article

Molecular Alterations and Expression Dynamics of LATS1 and LATS2 Genes in Non-Small-Cell Lung Carcinoma

verfasst von: Showkat A. Malik, Mosin S. Khan, Majeed Dar, Mahboob Ul Hussain, Mohammad A. Shah, Sheikh M. Shafi, Syed Mudassar

Erschienen in: Pathology & Oncology Research | Ausgabe 2/2018

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Abstract

Large tumor suppressor (LATS) is an important member of the Hippo pathway which can regulate organ size and cell proliferation. However, very little is known about the expression and clinical significance of LATS in lung cancer especially from this part of the world. We elucidated the frequency of LATS1 &LATS2 promoter hypermethylation (by methylation-specific PCR) and expression (by real-time PCR) in sixty nine (n = 69) Non-Small Cell Lung Cancer (NSCLC) patients and their corresponding normal lung tissue samples. We found promoter hypermethylation frequencies of LATS1 & LATS1to be 66.66% (46/69) and 71% (49/69) in NSCLC tissues. Decreased LATS1 & LATS2 mRNA expression was found in 55% and 66.66% of NSCLC patients. The LATS1 mRNA expression was significantly higher in normal lung tissues. Also, the mRNA levels of LATS1 and LATS2 NSCLC tissues with hypermethylation were significantly lower. Multivariable analysis confirmed that LATS1 under expression increased the hazard of death after adjusting for other clinicopathological factors. Importantly, the loss of LATS1 mRNA expression was associated with overall short survival. LATS1 is an independent prognostic factor and may play an important role in NSCLC progression and may serve as a novel therapeutic target of NSCLC.
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Metadaten
Titel
Molecular Alterations and Expression Dynamics of LATS1 and LATS2 Genes in Non-Small-Cell Lung Carcinoma
verfasst von
Showkat A. Malik
Mosin S. Khan
Majeed Dar
Mahboob Ul Hussain
Mohammad A. Shah
Sheikh M. Shafi
Syed Mudassar
Publikationsdatum
22.04.2017
Verlag
Springer Netherlands
Erschienen in
Pathology & Oncology Research / Ausgabe 2/2018
Print ISSN: 1219-4956
Elektronische ISSN: 1532-2807
DOI
https://doi.org/10.1007/s12253-017-0225-3

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