Can Glypican3 be Diagnostic for Early Hepatocellular Carcinoma among Egyptian Patients?

被引:29
作者
Abdelgawad, Iman Attia [1 ]
Mossallam, Ghada Ibrahim [1 ]
Radwan, Noha Hassan [1 ]
Elzawahry, Heba Mohammed [2 ]
Elhifnawy, Niveen Mostafa [1 ]
机构
[1] Cairo Univ, NCI, Dept Clin & Chem Pathol, Giza, Egypt
[2] Cairo Univ, NCI, Dept Med Oncol, Giza, Egypt
关键词
Glypican3; ELISA; RT/PCR; HCC; diagnosis; Egypt; MARKER; EXPRESSION; UTILITY; SERUM; HCC;
D O I
10.7314/APJCP.2013.14.12.7345
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Because of the high prevalence of hepatocellular carcinoma (HCC) in Egypt, new markers with better diagnostic performance than alpha-feto protein (AFP) are needed to help in early diagnosis. The aim of this work was to compare the clinical utility of both serum and mRNA glypican3 (GPC3) as probable diagnostic markers for HCC among Egyptian patients. Materials and Methods: A total of 60 subjects, including 40 with HCC, 10 with cirrhosis and 10 normal controls were analyzed for serum GPC3 (sGPC3) by ELISA. GPC-3 mRNA from circulating peripheral blood mononuclear cells was amplified by RT-PCR. Both markers were compared to some prognostic factors of HCC, and sensitivity of both techniques was compared. Results: Serum glypican-3 and AFP were significantly higher in the HCC group compared to cirrhotic and normal controls (p<0.001). Sensitivity and specificity were (95% each) for sGlypican-3, (82.5% and 85%) for AFP, and (100% and 90%) for Glypican3 mRNA, and (80% and 95%) for double combination between sGPC3 and AFP respectively. Conclusion: Both serum GPC-3 and GPC-3mRNA are promising diagnostic markers for early detection of HCC in Egyptian patients. RT-PCR proved to be more sensitive (100%) than ELISA (95%) in detecting glypican3.
引用
收藏
页码:7345 / 7349
页数:5
相关论文
共 26 条
  • [1] [Anonymous], INT J INTEGR BIOL
  • [2] [Anonymous], WORLD J MED SCI
  • [3] Changing pattern of hepatocellular carcinoma (HCC) and its risk factors in Egypt: Possibilities for prevention
    Anwar, Wagida A.
    Khaled, Hussein M.
    Amra, Hassan A.
    El-Nezami, Hani
    Loffredoe, Christopher A.
    [J]. MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2008, 659 (1-2) : 176 - 184
  • [4] El-Shenawy S Z, 2012, NAT SCI, V10, P32
  • [5] Filmus Jorge, 2004, Mol Diagn, V8, P207, DOI 10.2165/00066982-200408040-00002
  • [6] Identification of soluble NH2-terminal fragment of glypican-3 as a serological marker for early-stage hepatocellular carcinoma
    Hippo, Y
    Watanabe, K
    Watanabe, A
    Midorikawa, Y
    Yamamoto, S
    Ihara, S
    Tokita, S
    Iwanari, H
    Ito, Y
    Nakano, K
    Nezu, J
    Tsunoda, H
    Yoshino, T
    Ohizumi, I
    Tsuchiya, M
    Ohnishi, S
    Makuuchi, M
    Hamakubo, T
    Kodama, T
    Aburatani, H
    [J]. CANCER RESEARCH, 2004, 64 (07) : 2418 - 2423
  • [7] Iglesias BV, 2008, HISTOL HISTOPATHOL, V23, P1333, DOI 10.14670/HH-23.1333
  • [8] WT1 AS A NEW PROGNOSTIC FACTOR AND A NEW MARKER FOR THE DETECTION OF MINIMAL RESIDUAL DISEASE IN ACUTE-LEUKEMIA
    INOUE, K
    SUGIYAMA, H
    OGAWA, H
    NAKAGAWA, M
    YAMAGAMI, T
    MIWA, H
    KITA, K
    HIRAOKA, A
    MASAOKA, T
    NASU, K
    KYO, T
    DOHY, H
    NAKAUCHI, H
    ISHIDATE, T
    AKIYAMA, T
    KISHIMOTO, T
    [J]. BLOOD, 1994, 84 (09) : 3071 - 3079
  • [9] Glypican-3: From the mutations of Simpson-Golabi-Behmel genetic syndrome to a tumor marker for hepatocellular carcinoma
    Jakubovic, Baruch D.
    Jothy, Serge
    [J]. EXPERIMENTAL AND MOLECULAR PATHOLOGY, 2007, 82 (02) : 184 - 189
  • [10] Glypican-3 A Novel Diagnostic Marker for Hepatocellular Carcinoma and More
    Kandil, Dina H.
    Cooper, Kumarasen
    [J]. ADVANCES IN ANATOMIC PATHOLOGY, 2009, 16 (02) : 125 - 129