Expression pattern of the pendrin and sodium/iodide symporter genes in human thyroid carcinoma cell lines and human thyroid tumors

Eur J Endocrinol. 2001 Aug;145(2):129-35. doi: 10.1530/eje.0.1450129.

Abstract

Objective: In the present study we analyzed the pattern of pendrin (PDS) and sodium/iodide symporter (NIS) gene expression in some thyroid carcinoma cell lines and a series of thyroid tumoral tissues.

Methods: Total RNA was extracted from all cell lines and from 53 tissues, and gene expression was examined by RT-PCR. Semiquantitative 'multiplex' RT-PCR was used to assess variations in PDS gene expression among various thyroid pathologies. Pendrin expression was determined in the thyroid cell lines by Western blot analysis.

Results: PDS mRNA was expressed in all the cells investigated; conversely, NIS mRNA was detectable only in the B-CPAP cells. Pendrin protein was expressed in B-CPAP and WRO cell lines, reduced in FRO and absent in ARO cells. PDS gene expression was not detected in 5 of 25 differentiated thyroid carcinomas (DTC) while NIS gene was not expressed in six carcinomas. A concordance expression of both PDS and NIS transcripts was found in 20 DTC. In contrast, 2 neoplastic thyroid tissues carrying undetectable PDS mRNA maintained NIS transcript, and 3 thyroid carcinomas negative for NIS mRNA retained the expression of PDS gene. A semiquantitative analysis showed that the mean PDS mRNA levels were significantly decreased in DTC tissues.

Conclusions: Our data demonstrate that pendrin expression: (i) is present in the more differentiated thyroid carcinoma cell lines studied; (ii) is reduced or absent in DTC tissues; (iii) may not correlate with the NIS expression. These alterations may contribute to the loss of iodine concentration ability detected in thyroid tumors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma, Follicular / genetics*
  • Adenocarcinoma, Follicular / metabolism
  • Adenoma / genetics*
  • Adenoma / metabolism
  • Adult
  • Aged
  • Blotting, Western
  • Carcinoma, Papillary / genetics*
  • Carcinoma, Papillary / metabolism
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / genetics*
  • Female
  • Gene Expression
  • Gene Expression Regulation, Neoplastic / genetics*
  • Humans
  • Male
  • Membrane Proteins / biosynthesis
  • Membrane Proteins / genetics*
  • Membrane Transport Proteins*
  • Middle Aged
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sulfate Transporters
  • Symporters*
  • Thyroid Neoplasms / genetics*
  • Thyroid Neoplasms / metabolism
  • Tumor Cells, Cultured

Substances

  • Carrier Proteins
  • Membrane Proteins
  • Membrane Transport Proteins
  • RNA, Messenger
  • RNA, Neoplasm
  • SLC26A4 protein, human
  • Sulfate Transporters
  • Symporters
  • sodium-iodide symporter