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抑癌基因FHIT和PTEN在肝细胞癌中的表达及其意义 被引量:1

Expression and significance of anti-oncogene FHIT and PTEN in primary hepatocellular carcinoma
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摘要 目的:探讨FHIT和PTEN基因在肝细胞癌(HCC)中的表达及其意义。方法:采用免疫组化Envision二步法检测FHIT蛋白及PTEN蛋白在44例HCC组织及10例正常肝组织中的表达。结果:44例肝细胞癌组织中FHIT和PTEN蛋白的阴性表达率分别为38.6%(17/44)和47.7%(21/44),10例正常肝组织中FHIT和PTEN蛋白的阴性表达率均为0,两种抑癌基因在肝细胞癌组织与正常肝组织中的阴性表达率之间差异有统计学意义(P<0.05)。在HCC中FHIT基因的阴性表达率与HCC的病理分级、TNM临床分期和肿瘤直径有关(P<0.05),与AFP水平、HBsAg(+)和有无包膜无关(P>0.05)。PTEN蛋白的阴性表达率与病理分级显著相关(P<0.05),与TNM分期、肿瘤直径、AFP水平、HBsAg(+)和有无包膜无关(P>0.05)。相关性分析发现,FHIT和PTEN在HCC中的阴性表达呈正相关(rs=0.427,P<0.01)。分别比较FHIT和PTEN在HCC中蛋白阳性和阴性表达者的术后1、3年生存率,差异有统计学意义(P<0.05)。结论:FHIT和PTEN蛋白的异常表达与HCC的发生、发展有关,两者可能存在协同作用。FHIT可能是判断HCC恶性程度、侵袭能力和不良预后的重要指标,PTEN可能是判断HCC恶性程度和不良预后的指标。 Objective: To investigate the expression and significance of FHIT and PTEN in hepatocellular liver cancer (HCC). Methods: The expressions of FHIT and PTEN in 44 cases of HCC and 10 cases of normal liver tissues were detected by immunohistochemical Envision two-step method. Results: The negative expression rate of FHIT and FFEN were 38.6% (17/44) and 47.7% (21/44) respectively in 44 cases of HCC tissues and 0 in 10 cases of normal liver tissues, expres- sion of each anti-oncogene showed significant difference between HCC tissues and normal liver tissues (P〈0.05). The negative expression rate of FHIT in HCC was significantly associated with pathological grade, TNM stage and tumor diameter (P〈0.05), but was not associated with AFP level, HBsAg (+) or integral capsule (P〉0.05). The negative expression rate of PTEN was significantly associated with pathological grade (P〈0.05), but was not associated with TNM stage, AFP level, HBsAg (+) or integral capsule (P〉0.05). The negative expression of FHIT was positively correlated with the negative expression of PTEN in HCC (rs=0.427, P〈0.01). The difference was significant between the positive and negative expression of FHIT and PTEN and the survival rates of postoperative 1 year and 3 years. Conclusion: The results demonstrate that the abnormal expression of FHIT and PTEN may be correlated with the development and progression of HCC, and there is a synergistic action between the expression of FHIT and PTEN. FHIT may be used as an important marker of malignant degree, invasion capability and poor prognosis of HCC; PTEN may be used as an important marker of malignant degree and poor prognosis of HCC.
出处 《中国医药导报》 CAS 2010年第13期8-11,14,共5页 China Medical Herald
关键词 FHIT PTEN 肝细胞癌 免疫组织化学 FHIT PTEN Hepatocellular carcinoma Immunohistochemistry
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  • 1Croce CM, Sozzi G, Huebner K. Role of FHIT in human cancer. J Clin Oncol 1999; 17:1618-1624.
  • 2Huebner K, Druck T, Siprashvili Z, Croce CM, Kovatich A,McCue PA. The role of deletions at the FRA3B/FHIT locus in carcinogenesis. Recent Results Cancer Res 1998; 154:200-215.
  • 3Sorio C, Baron A, Orlandini S, Zamboni G, Pederzoli P, Huebner K, Scarpa A. The FHIT gene is expressed in pancreatic ductular cells and is altered in pancreatic cancers. Cancer Res 1999; 59:1308-1314.
  • 4Hadaczek P, Siprashvili Z, Markiewski M, Domagala W, Druck T, McCue PA, Pekarsky Y, Ohta M, Huebner K, Lubinski J. Absence or reduction of Fhit expression in most clear cell renal carcinomas. Cancer Res 1998; 58:2946-2951.
  • 5Werner NS, Siprashvili Z, Fong LY, Marquitan G, Schroder JK,Bardenheuer W, Seeber S, Huebner K, Schutte J, Opalka B. Differential susceptibility of renal carcinoma cell lines to tumor suppression by exogenous Fhit expression. Cancer Res 2000; 60:2780-2785.
  • 6Greenspan DL, Connolly DC, Wu R, Lei RY, Vogelstein JT, Kim YT, Mok JE, Munoz N, Bosch FX, Shah K, Cho KR. Loss of FHIT expression in cervical carcinoma cell lines and primary tumors.Cancer Res 1997; 57:4692-4698.
  • 7Yoshino K, Enomoto T, Nakamura T, Nakashima R, Wada H,Saitoh J, Noda K, Murata Y. Aberrant FHIT transcripts in squamous cell carcinoma of the uterine cervix. Int J Cancer 1998; 76:176-181.
  • 8Druck T, Berk L, Huebner K. FHITness and cancer. Oncol Res 1998; 10:341-345.
  • 9Fong KM, Biesterveld EJ, Virmani A, Wistuba I, Sekido Y, Bader SA, Ahmadian M, Ong ST, Rassool FV, Zimmerman PV, Giaccone G, Gazdar A.F, Minna JD. FHIT and FRA3B 3p14.2 allele loss are common in lung cancer and preneoplastic bronchial lesions and are associated with cancer-related FHIT cDNA splicing aberrations. Cancer Res 1997; 57:2256-2267.
  • 10Sozzi G, Tornielli S, Tagliabue E, Sard L, Pezzella F, Pastorino U, Minoletti F, Pilotti S, Ratcliffe C, Veronese ML, Goldstraw P,Huebner K, Croce CM, Pierotti MA. Absence of Fhit protein in primary lung tumors and cell lines with FHIT gene abnormalities.Cancer Res 1997; 57:5207-5212.

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