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人端粒酶逆转录酶基因表达在甲状腺滤泡性肿瘤细针穿刺原位杂交中的临床应用

Clinical application of human telomerase reverse transcriptase gene expression in thyroid follicular tumors by fine-needle aspirations using in situ hybridization.

作者信息

Kammori Makoto, Nakamura Ken-Ichi, Hashimoto Masanori, Ogawa Toshihisa, Kaminishi Michio, Takubo Kaiyo

机构信息

Division of Breast Cancer Surgery, Department of Surgery, The University of Tokyo, Japan.

出版信息

Int J Oncol. 2003 May;22(5):985-91.

Abstract

Most of fine-needle aspiration (FNA) biopsies for follicular tumors of the thyroid are deemed 'indeterminate' or 'suspicious' with regard to malignancy, even though most of these lesions are benign. Therefore, additional diagnostic markers of malignancy are needed. Telomerase activity is present in most malignant tumors. Expression of the gene encoding human telomerase reverse transcriptase (hTERT) is very closely associated with telomerase activity, this gene is overexpressed in most thyroid carcinomas. We examined telomerase activity by the telomeric repeat amplification protocol (TRAP) and hTERT gene expression by in situ hybridization (ISH) in thyroid tissue including 6 follicular carcinomas and 15 follicular adenomas. ISH for hTERT gene was performed using FNA samples from the same patients. Telomerase activity was detected in all six of the follicular carcinomas and in five (33%) of the 15 follicular adenoma tissue specimens. hTERT gene expression was detected the follicular cancer cells in all of the lesions and in one (7%) of the 15 thyroid adenomas. Moreover, we demonstrated that hTERT gene expression was occurring in four (67%) of the 6 follicular carcinoma biopsy specimens obtained using FNA. These results suggest that the detection of hTERT gene expression using ISH tissue specimens can be used to distinguish between benign and malignant follicular lesions of the thyroid, however the detection of hTERT gene in FNA samples using ISH cannot be used to definitively diagnose follicular tumors of the thyroid.

摘要

大多数甲状腺滤泡性肿瘤的细针穿刺(FNA)活检在恶性方面被判定为“不确定”或“可疑”,尽管这些病变大多数是良性的。因此,需要额外的恶性诊断标志物。大多数恶性肿瘤中存在端粒酶活性。编码人端粒酶逆转录酶(hTERT)的基因表达与端粒酶活性密切相关,该基因在大多数甲状腺癌中过度表达。我们通过端粒重复序列扩增法(TRAP)检测端粒酶活性,并通过原位杂交(ISH)检测包括6例滤泡癌和15例滤泡性腺瘤在内的甲状腺组织中的hTERT基因表达。使用来自同一患者的FNA样本进行hTERT基因的ISH检测。在所有6例滤泡癌以及15例滤泡性腺瘤组织标本中的5例(33%)中检测到端粒酶活性。在所有病变的滤泡癌细胞以及15例甲状腺腺瘤中的1例(7%)中检测到hTERT基因表达。此外,我们证明在使用FNA获得的6例滤泡癌活检标本中的4例(67%)中发生了hTERT基因表达。这些结果表明,使用ISH组织标本检测hTERT基因表达可用于区分甲状腺滤泡性良性和恶性病变,然而使用ISH检测FNA样本中的hTERT基因不能用于明确诊断甲状腺滤泡性肿瘤。

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