Sugg S L, Ezzat S, Zheng L, Freeman J L, Rosen I B, Asa S L
Department of Surgery, Mount Sinai Hospital, Toronto, Ontario, Canada.
Surgery. 1999 Jan;125(1):46-52.
Our purpose was to study the expression of multiple oncogenes in papillary thyroid cancer for possible interactions and prognostic significance.
Twenty papillary thyroid carcinomas were studied for expression/mutation of 3 oncogenes: ras, ret/PTC, and erbB-2/neu. H, N, and K ras codons were examined by polymerase chain reaction (PCR), single-stranded conformation polymorphism, and sequencing. The thyroid oncogene ret/PTC was identified by reverse transcription (RT)-PCR. Gene amplification of erbB-2/neu was analyzed by differential PCR. The transmembrane domain of erbB-2/neu was sequenced for activating mutations. Quantitation of erbB-2/neu mRNA was evaluated by competitive RT-PCR, and protein expression was determined by immunohistochemistry.
Among 20 tumors, 3 had insular/anaplastic dedifferentiation, 13 were intrathyroidal, and 7 were metastatic to cervical lymph nodes (6) or lung (1). An H-ras 13 mutation was found in 1 metastatic tumor and an N-ras 61 mutation in 1 intrathyroidal tumor. ret/PTC was identified in 3 intrathyroidal and 5 metastatic tumors. No erbB-2/neu DNA amplification or mutations were identified, although 4 tumors had elevated erbB-2/neu mRNA levels. Three of 20 patients had abnormalities detected in multiple oncogenes; 2 had elevated erbB-2/neu mRNA and ret/PTC rearrangements, and 1 of these had pulmonary metastasis. An intrathyroidal papillary cancer had an N61 ras mutation and a ret/PTC gene rearrangement.
ret/PTC rearrangements are present in 40% of papillary thyroid carcinomas and may play a role in metastatic behavior. In contrast, ras mutations are rare (10%). erbB-2/neu gene amplification and activating mutations are not detected, although elevated mRNA levels were found in 20% of papillary carcinomas. The lack of correlation among the 3 oncogenes in 17 of 20 (85%) papillary thyroid carcinomas suggests that they were not cumulative factors in the pathogenesis of these tumors.
我们的目的是研究甲状腺乳头状癌中多种癌基因的表达情况,以探讨其可能的相互作用及预后意义。
对20例甲状腺乳头状癌进行研究,检测3种癌基因的表达/突变情况:ras、ret/PTC和erbB-2/neu。通过聚合酶链反应(PCR)、单链构象多态性分析和测序检测H、N和K ras密码子。通过逆转录(RT)-PCR鉴定甲状腺癌基因ret/PTC。通过差异PCR分析erbB-2/neu的基因扩增情况。对erbB-2/neu的跨膜结构域进行测序以检测激活突变。通过竞争性RT-PCR评估erbB-2/neu mRNA的定量,通过免疫组织化学测定蛋白表达。
20例肿瘤中,3例为岛状/间变性去分化,13例局限于甲状腺内,7例转移至颈部淋巴结(6例)或肺(1例)。在1例转移瘤中发现H-ras 13突变,在1例甲状腺内肿瘤中发现N-ras 61突变。在3例甲状腺内肿瘤和5例转移瘤中鉴定出ret/PTC。未发现erbB-2/neu DNA扩增或突变,尽管4例肿瘤的erbB-2/neu mRNA水平升高。20例患者中有3例在多种癌基因中检测到异常;2例erbB-2/neu mRNA升高且ret/PTC重排,其中1例有肺转移。1例甲状腺内乳头状癌有N61 ras突变和ret/PTC基因重排。
ret/PTC重排在40%的甲状腺乳头状癌中存在,可能在转移行为中起作用。相比之下,ras突变很少见(10%)。未检测到erbB-2/neu基因扩增和激活突变,尽管在20%的乳头状癌中发现mRNA水平升高。20例(85%)甲状腺乳头状癌中有17例的3种癌基因之间缺乏相关性,提示它们不是这些肿瘤发病机制中的累积因素。