Literature DB >> 22373659

Differential expression of PAI-RBP1, C1orf142, and COTL1 in non-small cell lung cancer cell lines with different tumor metastatic potential.

Wenjing Sun1, Changlong Guo, Xiangning Meng, Yang Yu, Yan Jin, Dandan Tong, Jingshu Geng, Qi Huang, Jiping Qi, An Liu, Rongwei Guan, Lidan Xu, Donglin Sun, Wei Ji, Peng Liu, Fangli Liu, Haiming Sun, Guohua Ji, Songbin Fu, Jing Bai.   

Abstract

Human non-small cell lung cancer (NSCLC) is one of the most common malignancies in the modern world. Its recurrence is mainly due to its ability to invade and metastasize. However, the precise mechanism for tumor development and metastasis is still not fully understood. To shed light on the development of lung cancer, the human giant cell lung carcinoma cell lines 95D with high metastatic potential and 95C with low metastatic potential were selected in this study. The 2 cell lines originated from the same parental cell and share a similar genetic background. In the current study, we identified 3 differentially expressed proteins in 95C and 95D cell lines, namely, PAI-RBP1, C1orf142, and COTL1, by using 2-dimensional electrophoresis proteomics analysis. We found that PAI-RBP1 and C1orf142 expression levels were higher in 95D than in 95C cells, whereas COTL1 expression level was lower in 95D when compared to 95C cells. We also confirmed these results by reverse transcription-polymerase chain reaction and immunoblotting analyses. The messenger RNA and protein levels of PAI-RBP1 and C1orf142 were much higher in 95D than in 95C cells, and COTL1 expression level was lower in 95D than in 95C cells. The PAI-RBP1 expression was assessed by immunohistochemistry in 70 NSCLC and 7 normal lung tissue samples from patients. PAI-RBP1 expression level was higher in tumor tissues (positive staining in 87.1% of cases [61/70]) than in normal tissues (positive staining in 14.3% of cases [1/7]). In conclusion, by studying protein expression in NSCLC cell lines with high and low metastasis as well as in human lung cancer tissues, we have identified 3 proteins, namely, PAI-RBP1, C1orf142, and COTL1, which were differentially expressed in NSCLC cell lines with different metastatic potential. In addition, we also found that PAI-RBP1 might contribute to NSCLC development.

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Year:  2012        PMID: 22373659     DOI: 10.2310/JIM.0b013e31824963b6

Source DB:  PubMed          Journal:  J Investig Med        ISSN: 1081-5589            Impact factor:   2.895


  12 in total

1.  Coactosin-like protein CLP/Cotl1 suppresses breast cancer growth through activation of IL-24/PERP and inhibition of non-canonical TGFβ signaling.

Authors:  L Xia; X Xiao; W L Liu; Y Song; T J J Liu; Y J Li; E Zacksenhaus; X J Hao; Y Ben-David
Journal:  Oncogene       Date:  2017-09-18       Impact factor: 9.867

2.  Downregulation of microRNA-30c-5p was responsible for cell migration and tumor metastasis via COTL1-mediated microfilament arrangement in breast cancer.

Authors:  Bei Pei; Tongyang Li; Qi Qian; Wenqiang Fan; Xiao He; Yulan Zhu; Lingyun Xu
Journal:  Gland Surg       Date:  2020-06

3.  Coactosin-Like Protein in Breast Carcinoma: Friend or Foe?

Authors:  Bei Wang; Limiao Zhao; Dandan Chen
Journal:  J Inflamm Res       Date:  2022-07-15

4.  microRNA-548l is involved in the migration and invasion of non-small cell lung cancer by targeting the AKT1 signaling pathway.

Authors:  Caihong Liu; Huan Yang; Zhijie Xu; Dan Li; Meiyu Zhou; Kui Xiao; Zhihui Shi; Lanyan Zhu; Lifang Yang; Rui Zhou
Journal:  J Cancer Res Clin Oncol       Date:  2014-09-23       Impact factor: 4.553

5.  SERBP1 affects homologous recombination-mediated DNA repair by regulation of CtIP translation during S phase.

Authors:  Jang-Won Ahn; Sunjik Kim; Wooju Na; Su-Jin Baek; Jeong-Hwan Kim; Keehong Min; Jeonghun Yeom; Hoyun Kwak; Sunjoo Jeong; Cheolju Lee; Seon-Young Kim; Cheol Yong Choi
Journal:  Nucleic Acids Res       Date:  2015-06-11       Impact factor: 16.971

6.  Retrospective Proteomic Screening of 100 Breast Cancer Tissues.

Authors:  Ida Pucci-Minafra; Gianluca Di Cara; Rosa Musso; Patrizia Cancemi; Nadia Ninfa Albanese; Elena Roz; Salvatore Minafra
Journal:  Proteomes       Date:  2017-07-07

7.  Functional Modulation of Gene Expression by Ultraconserved Long Non-coding RNA TUC338 during Growth of Human Hepatocellular Carcinoma.

Authors:  Hui-Ju Wen; Michael P Walsh; Irene K Yan; Kenji Takahashi; Alan Fields; Tushar Patel
Journal:  iScience       Date:  2018-04-27

Review 8.  Complex interactomes and post-translational modifications of the regulatory proteins HABP4 and SERBP1 suggest pleiotropic cellular functions.

Authors:  Carolina Colleti; Talita Diniz Melo-Hanchuk; Flávia Regina Moraes da Silva; Ângela Saito; Jörg Kobarg
Journal:  World J Biol Chem       Date:  2019-11-21

9.  Antitumor mechanisms of amino Acid hydroxyurea derivatives in the metastatic colon cancer model.

Authors:  Nina Saban; Višnja Stepanić; Srđan Vučinić; Anita Horvatić; Mario Cindrić; Ivana Perković; Branka Zorc; Nada Oršolić; Mladen Mintas; Krešimir Pavelić; Sandra Kraljević Pavelić
Journal:  Int J Mol Sci       Date:  2013-12-04       Impact factor: 5.923

10.  Expression of Progesterone Receptor Membrane Component 1 (PGRMC1), Progestin and AdipoQ Receptor 7 (PAQPR7), and Plasminogen Activator Inhibitor 1 RNA-Binding Protein (PAIRBP1) in Glioma Spheroids In Vitro.

Authors:  Juraj Hlavaty; Reinhard Ertl; Ingrid Miller; Cordula Gabriel
Journal:  Biomed Res Int       Date:  2016-06-01       Impact factor: 3.411

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