Title of article
Connexin26 expression is associated with aggressive phenotype in human papillary and follicular thyroid cancers
Author/Authors
Naoi، نويسنده , , Yasuto and Miyoshi، نويسنده , , Yasuo and Taguchi، نويسنده , , Tetsuya and Kim، نويسنده , , Seung Jin and Arai، نويسنده , , Takashi and Maruyama، نويسنده , , Naomi and Tamaki، نويسنده , , Yasuhiro and Noguchi، نويسنده , , Shinzaburo، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2008
Pages
9
From page
248
To page
256
Abstract
Connexin26 (Cx26), a component of GAP junctions and until recently believed to be a tumor suppressor gene, has been shown to play an important role in lymphatic invasion as well as lymph node and distant metastases in squamous lung cancer and breast cancer. In the study presented here, we investigated Cx26 expression in human papillary thyroid cancer (PTC) and follicular thyroid cancer (FTC) and its relationship with various clinicopathological parameters. Of 69 PTCs, 33 were positive for Cx26 (47.8%), as were five of 11 FTCs (45.5%), all follicular thyroid adenomas (n = 22) and normal thyroid tissues (n = 20) were negative for Cx26. A statistically significant association was observed between Cx26 expression and large tumor size (p = 0.028 for PTC) and lymph node metastases (p = 0.053 (marginally significant) for PTC and p = 0.035 for FTC). Presence of intra-glandular dissemination of tumor cells was significantly (p = 0.048) more frequent in Cx26-positive (30.3%) than Cx26-negative PTCs (11.1%). Lymphatic vessel invasion was more frequent in Cx26-positive PTCs (6.1%) than in Cx26-negative PTCs (0%) though the difference was not statistically significant. These results suggest that Cx26 may be implicated in the pathogenesis of PTC and FTC and is associated with the biologically aggressive phenotypes of these tumors.
Keywords
Thyroid cancer , D2-40 , Connexin26 , CD34
Journal title
Cancer Letters
Serial Year
2008
Journal title
Cancer Letters
Record number
1811707
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