Serum Laminin γ2 Monomer as a Diagnostic and Predictive Biomarker for Hepatocellular Carcinoma

被引:21
|
作者
Yamashita, Taro [1 ,2 ]
Koshikawa, Naohiko [3 ,4 ,5 ]
Shimakami, Tetsuro [2 ]
Terashima, Takeshi [2 ]
Nakagawa, Masatoshi [6 ]
Nio, Kouki [2 ]
Horii, Rika [2 ]
Iida, Noriho [2 ]
Kawaguchi, Kazunori [2 ]
Arai, Kuniaki [2 ]
Sakai, Yoshio [2 ]
Yamashita, Tatsuya [2 ]
Mizukoshi, Eishiro [2 ]
Honda, Masao [2 ]
Kitao, Azusa [7 ]
Kobayashi, Satoshi [7 ]
Takahara, Shizuko [8 ]
Imai, Yasuhito [8 ]
Yoshimura, Kenichi [8 ,9 ]
Murayama, Toshinori [8 ]
Nakamoto, Yasunari [10 ]
Yoshida, Eisaku [6 ]
Yoshimura, Toru [6 ]
Seiki, Motoharu [11 ]
Kaneko, Shuichi [2 ]
机构
[1] Kanazawa Univ Hosp, Dept Gen Med, 13-1 Takara Machi, Kanazawa, Ishikawa 9208641, Japan
[2] Kanazawa Univ Hosp, Dept Gastroenterol, Kanazawa, Ishikawa, Japan
[3] Kanagawa Canc Ctr Res Inst, Div Canc Cell Res, Yokohama, Kanagawa, Japan
[4] Univ Tokyo, Inst Med Sci, Tokyo, Japan
[5] Tokyo Inst Technol, Dept Life Sci & Technol, Yokohama, Kanagawa, Japan
[6] Abbott Japan LLC, Diagnost Div, Matsudo, Chiba, Japan
[7] Kanazawa Univ Hosp, Dept Radiol, Kanazawa, Ishikawa, Japan
[8] Kanazawa Univ, Kanazawa Univ Hosp, Innovat Clin Res Ctr, Kanazawa, Ishikawa, Japan
[9] Hiroshima Univ Hosp, Ctr Integrated Med Res, Hiroshima, Japan
[10] Univ Fukui, Dept Internal Med 2, Sch Med Sci, Fukui, Japan
[11] Kanazawa Univ, Fac Med, Inst Med Pharmaceut & Hlth Sci, Kanazawa, Ishikawa, Japan
关键词
LIVER-CANCER; HEPATITIS-C; STEM-CELLS; EPCAM;
D O I
10.1002/hep.31758
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUNDS AND AIMS: Structural dynamics of basement membrane components are still to be elucidated in the process of hepatocarcinogenesis. We evaluated the characteristics of HCC expressing laminin gamma 2 monomer (LG2m), a basement membrane component not detected in normal tissues, for I ICC diagnosis. We further determined whether elevated serum LG2m is a risk factor for HCC development in patients with chronic hepatitis C (CHC). APPROACH AND RESULTS: In HCC cell lines, LG2m was expressed in alpha-fetoprotein (AFP)-negative, CD90-positive cells characterized by highly metastatic natures. Using 14 cell lines and 258 HCC microarray data, we identified that LG2m gene signature was associated with Hoshida's S1/Boyault's G3 molecular subclasses with poor prognosis, which could not be recognized by AFP. Serum LG2m was assessed in 24 healthy donors, 133 chronic liver disease patients, and 142 HCC patients, and sensitivity and specificity of LG2m testing for HCC diagnosis were 62.9% and 70.5%, respectively (cutoff, 30 pg/mL). We evaluated the consequence of LG2m elevation in two independent HCC cohorts (n = 47 and n = 81), and LG2m-high HCC showed poor prognosis with later development of distant organ metastasis (cutoff, 60 pg/mL). LG2m was slightly elevated in a subset of CHC patients, and Kaplan-Meier analysis indicated a high incidence of HCC (n = 70). For validation, we enrolled 399 CHC patients with sustained virological response (SVR) as a multicenter, prospective study, and serum LG2m elevation correlated with a high incidence of HCC in the CHC patients with SVR (P < 0.0001). CONCLUSIONS: LG2m is a predictive biomarker for the development of metastatic HCC. Elevated serum LG2m is an HCC risk in CHC patients who have achieved SVR.
引用
收藏
页码:760 / 775
页数:16
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