Literature DB >> 28351304

Expression of lactate dehydrogenase C correlates with poor prognosis in renal cell carcinoma.

Yibo Hua1, Chao Liang1, Jundong Zhu1, Chenkui Miao1, Yajie Yu1, Aimin Xu1, Jianzhong Zhang1, Pu Li1, Shuang Li1, Meiling Bao2, Jie Yang1, Chao Qin1, Zengjun Wang1.   

Abstract

Lactate dehydrogenase C is an isoenzyme of lactate dehydrogenase and a member of the cancer-testis antigens family. In this study, we aimed to investigate the expression and functional role of lactate dehydrogenase C and its basic mechanisms in renal cell carcinoma. First, a total of 133 cases of renal cell carcinoma samples were analysed in a tissue microarray, and Kaplan-Meier survival curve analyses were performed to investigate the correlation between lactate dehydrogenase C expression and renal cell carcinoma progression. Lactate dehydrogenase C protein levels and messenger RNA levels were significantly upregulated in renal cell carcinoma tissues, and the patients with positive lactate dehydrogenase C expression had a shorter progression-free survival, indicating the oncogenic role of lactate dehydrogenase C in renal cell carcinoma. In addition, further cytological experiments demonstrated that lactate dehydrogenase C could prompt renal cell carcinoma cells to produce lactate, and increase metastatic and invasive potential of renal cell carcinoma cells. Furthermore, lactate dehydrogenase C could induce the epithelial-mesenchymal transition process and matrix metalloproteinase-9 expression. In summary, these findings showed lactate dehydrogenase C was associated with poor prognosis in renal cell carcinoma and played a pivotal role in the migration and invasion of renal cell carcinoma cells. Lactate dehydrogenase C may act as a novel biomarker for renal cell carcinoma progression and a potential therapeutic target for the treatment of renal cell carcinoma.

Entities:  

Keywords:  Lactate dehydrogenase C; cancer–testis antigens; epithelial–mesenchymal transition; renal cell carcinoma; tumour metastasis

Mesh:

Substances:

Year:  2017        PMID: 28351304     DOI: 10.1177/1010428317695968

Source DB:  PubMed          Journal:  Tumour Biol        ISSN: 1010-4283


  13 in total

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