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Authors Wu YY, Liu XY, Zhuo DX, Huang HB, Zhang FB, Liao SF
Received 24 February 2018
Accepted for publication 20 April 2018
Published 22 June 2018 Volume 2018:10 Pages 1647—1655
DOI https://doi.org/10.2147/CMAR.S166390
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Amy Norman
Peer reviewer comments 2
Editor who approved publication: Dr Leylah Drusbosky
Purpose: The
aim of this study was to investigate whether the expression of the ligand-gated
Ca2+channel transient
receptor potential vanilloid type-1 (TRPV1) in primary human renal cell
carcinoma (RCC) is associated with clinicopathological features.
Patients and
methods: Fresh and frozen primary tumor and
normal peritumoral kidney tissues from 127 patients diagnosed with RCC were
analyzed for TRPV1 expression by quantitative reverse transcription polymerase
chain reaction (RT-PCR), Western blotting and immunohistochemistry.
Results: Quantitative RT-PCR revealed that TRPV1 was decreased 3.20-fold in RCC
tissue vs normal peritumoral kidney tissue (p =0.012).
Significantly different TRPV1 mRNA expression was detected in RCC tissues of
different Fuhrman grades and histopathological subtypes (F=4.282, p =0.015 and F=5.205, p =0.014, respectively). Decreased
TRPV1 expression was correlated with RCC histopathological subtype
(R=-0.554, p =0.003) and Fuhrman grade
(R=−0.525, p =0.006). Western blot analysis of
TRPV1 protein expression showed similar results. Immunohistochemical analysis
showed strong expression of TRPV1 in kidney tubules but demonstrated weak or no
immunostaining in RCC tissues.
Conclusion: TRPV1 expression was decreased in RCC, which was significantly
associated with tumor Fuhrman grades and histopathological subtypes. It seems
to suggest that TRPV1 expression may be a valuable tool to predict the extent
of RCC progression.
Keywords: renal cell carcinoma, TRPV1, Fuhrman grade, histopathological
subtype, prognostic factor