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肾上腺嗜铬细胞瘤中c-myc、bcl-2 mRNA表达及意义的研究 被引量:1

Expression and Significance of c-myc、bcl-2 mRNA in Human adrenal pheochromocytomas
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摘要 目的 探讨癌基因c -myc、凋亡抑制基因bcl-2mRNA在肾上腺良性及恶性嗜铬细胞瘤中的表达及其意义。方法 应用核酸分子原位杂交方法检测 2 9例良性肾上腺嗜铬细胞瘤及 7例恶性肾上腺嗜铬细胞瘤中c -myc、bcl-2基因表达情况。结果 原位杂交结果显示 :c -mycmRNA在良、恶性肾上腺嗜铬细胞瘤中表达率分别为2 7.5 % (8 2 9) ,71.4% (5 7) (P <0 .0 5 ) ;bcl-2mRNA在良性肾上腺嗜铬细胞瘤中表达率分别为 48.2 % (14 2 9,71.4%(5 7) ,两者比较存在显著性差异 (P <0 .0 5 )。结论  1、c -myc在肾上腺嗜铬细胞瘤的发生过程中c -myc基因不起主要作用 ,可能对该肿瘤的恶性变起重要作用 ,c -myc基因产物的检测对鉴别良、恶性肾上腺嗜铬细胞瘤有一定意义。 2、bcl-2基因的凋亡抑制作用对肾上腺嗜铬细胞瘤的发生发展有重要意义 ,但在良、恶性肾上腺嗜铬细胞瘤的鉴别上无临床意义。 Objective:The expression of c-myc?bcl-2 in human adernal pheochromocytmas were studied at mRNA levels.Methods:29 cases of benign pheochromocytomas and 7 cases of malignant pheochromocytomas were studied with in situ hybridization methods.Results:c-myc mRNA positive rate in 29 cases of benign and 7 cases of malignant adrenal pheochromocytomas were 27.5%(8/29) and 71.4%(5/7)(P<0.05).bcl-2 mRNA positive rate in 29 cases of benign and 7 cases of malignant adrenal pheochromocytomas were 48.2%(14/29) and 71.4%(5/7)(P<0.05).Conclusion:1. c-myc is closely related with the occurrence and development of malignant adrenal pheochromocytomas;The detection of c-myc in pheochromocytomas might be useful in differentiation of malignant from benign pheochromocytomas.2? bcl-2 overexpression is closely related to pathogenesis of adrenal pheochromocytomas.but the detection of bcl-2 in pheochromocytmas might not be useful in differentiation of malignant from benign pheochromocytmas.
出处 《海南医学》 CAS 2003年第3期4-6,共3页 Hainan Medical Journal
关键词 肾上腺嗜铬细胞瘤 c—myc 调亡抑制基因 bcl—2 良性 恶性 核酸分子 原位杂交 mRNA pheochromocytomas c-myc gene bcl-2 gene in situ hybridization
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  • 1刘彤华,陈原稼,武莎菲,高洁,蒋卫君,卢朝辉,关键,魏拴增,罗玉凤,曹金玲,万建伟.良性和恶性嗜铬细胞瘤的区别[J].中华病理学杂志,2004,33(3):198-202. 被引量:29
  • 2Mebta RR, McDermott JH, Hieken TJ, et al. Plasma c-erbB2 levels in breast cancer patients: prognostic significance in predicting response to chemotherapy. J Clin Oncol, 1998,16: 2409-2416.
  • 3Castilla-Guerra L, Moreno AM, Frenandez-moreno MC, et al. Expression and prognostic value of c-erbB-2 oncogene product in human pheochromocytomas. Histopathology, 1997,31 : 144-149.
  • 4Fanidi A, Harrington EA, Evan GI. Cooperative interaction between c-myc and bcl-2 proto-oncogenes. Nature, 1992,359:554- 556.
  • 5Wang DG, Johnston CF, Marley J J, et al. Expression of the apoptosis-suppressing gene Bcl-2 in pheochromocytoma is associated with the expression of c-myc. J Clin Endocrinol Metab, 1997,82: 1949-1952.
  • 6Newmann MD, Bausch B, McWhinney SR, et al. Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J Med,2002, 346 : 1459-1466.
  • 7Maier-Woelfle M, Brandle M, Komminoth P, et al. A novel succinate dehydrogenase subunit B gene mutation, H132P, causes familial malignant sympathetic extraadrenal paragangliomas. J Clin Endocrinol Metab,2004,89:362-367.
  • 8Brouwers FM, Eisenhofer G, Tao JJ, et al. High Frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing. J Clin Endocrinol Metab,2006,91:4505-4509.
  • 9Gimenez-Roqueplo AP, Favier J, Rustin P, et al. Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. Cancer Res, 2003, 63:5615-5621.
  • 10DeLellis RA, Lloyd RV, Heitz PU, et al. Pathology and Genetics: World Health Organization Classification of Tumours of Endocrine Organs. England: Oxford University Press, 2004.

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