Biomarkers for hepatocellular carcinoma: diagnostic and therapeutic utility

被引:38
作者
Ferrin, Gustavo [1 ,2 ]
Aguilar-Melero, Patricia [1 ]
Rodriguez-Peralvarez, Manuel [1 ,2 ]
Luis Montero-Alvarez, Jose [1 ,2 ]
de la Mata, Manuel [1 ,2 ]
机构
[1] Hosp Univ Reina Sofia, Liver Unit, Inst Maimonides Invest Biomed Cordoba IMIBIC, Avda Menendez Pidal S-N, Cordoba 14004, Spain
[2] Inst Salud Carlos III, Enfermedades Hepat & Digest, CIBER, Madrid, Spain
关键词
diagnosis; sorafenib; therapy;
D O I
10.2147/HMER.S50161
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Because of the high prevalence and associated-mortality of hepatocellular carcinoma (HCC), early diagnosis of the disease is vital for patient survival. In this regard, tumor size is one of the two main prognostic factors for surgical resection, which constitutes the only curative treatment for HCC along with liver transplantation. However, techniques for HCC surveillance and diagnosis that are currently used in clinical practice have certain limitations that may be inherent to the tumor development. Thus, it is important to continue efforts in the search for biomarkers that increase diagnostic accuracy for HCC. In this review, we focus on different biological sources of candidate biomarkers for HCC diagnosis. Although those biomarkers identified from biological samples obtained by noninvasive methods have greater diagnostic value, we have also considered those obtained from liver tissue because of their potential therapeutic value. To date, sorafenib is the only US Food and Drug Administration-approved antineoplastic for HCC. However, this therapeutic agent shows very low tumor response rates and frequently causes acquired resistance in HCC patients. We discuss the use of HCC biomarkers as therapeutic targets themselves, or as targets to increase sensitivity to sorafenib treatment.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 108 条
[41]   Elevated plasma osteopontin levels in patients with hepatocellular carcinoma [J].
Kim, Jin ;
Ki, Seung S. ;
Lee, Sang D. ;
Han, Chul J. ;
Kim, Yu C. ;
Park, Sun H. ;
Cho, Soo Y. ;
Hong, Young-Joon ;
Park, Hyo Y. ;
Lee, Myoungjin ;
Jung, Ha H. ;
Lee, Kee H. ;
Jeong, Sook-Hyang .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2006, 101 (09) :2051-2059
[42]  
Koike Y, 2001, CANCER, V91, P561, DOI 10.1002/1097-0142(20010201)91:3<561::AID-CNCR1035>3.0.CO
[43]  
2-N
[44]   Pathologic Diagnosis of Early Hepatocellular Carcinoma: A Report of the International Consensus Group for Hepatocellular Neoplasia [J].
Kojiro, Masamichi ;
Wanless, Ian R. ;
Alves, Venancio ;
Badve, Sunil ;
Bala-baud, Charles ;
Bedosa, Pierre ;
Bhathal, Prithi ;
Bioulac-Sage, Paulette ;
Brunt, Elizabeth M. ;
Burt, Alastair D. ;
Craig, John R. ;
Dhillon, Amar ;
Ferrell, Linda ;
Geller, Stephen A. ;
Goodman, Zackary D. ;
Gouw, Annette S. H. ;
Guido, Maria ;
Guindi, Maha ;
Hytiroglou, Prodromos ;
Kage, Masayoshi ;
Kondo, Fukuo ;
Kudo, Masutoshi ;
Lauwers, Gregory Y. ;
Nakano, Masayuki ;
Paradis, Valerie ;
Park, Young-Nyun ;
Quaglia, Alberto ;
Roncalli, Massimo ;
Roskams, Tania ;
Ruebner, Boris ;
Sakamoto, Michiie ;
Sax-ena, Romil ;
Theise, Neil D. ;
Thung, Swan ;
Toniakos, Dina .
HEPATOLOGY, 2009, 49 (02) :658-664
[45]   Alterations of DNA methylation and histone modifications contribute to gene silencing in hepatocellular carcinomas [J].
Kondo, Yutaka ;
Shen, Lanlan ;
Suzuki, Seiji ;
Kurokawa, Tsuyoshi ;
Masuko, Kazuo ;
Tanaka, Yasuhito ;
Kato, Hideaki ;
Mizuno, Yoshiki ;
Yokoe, Masamichi ;
Sugauchi, Fuminaka ;
Hirashima, Noboru ;
Orito, Etsuro ;
Osada, Hirotaka ;
Ueda, Ryuzo ;
Guo, Yi ;
Chen, Xinli ;
Issa, Jean-Pierre J. ;
Sekido, Yoshitaka .
HEPATOLOGY RESEARCH, 2007, 37 (11) :974-983
[46]  
KUROMATSU R, 1993, LIVER, V13, P177
[47]   Monoclonal Antibody Targeting of the Cell Surface Molecule TM4SF5 Inhibits the Growth of Hepatocellular Carcinoma [J].
Kwon, Sanghoon ;
Choi, Kyung-Chan ;
Kim, Young-Eun ;
Ha, Yang-Wha ;
Kim, Dongbum ;
Park, Byoung Kwon ;
Wu, Guang ;
Kim, Doo-Sik ;
Lee, Younghee ;
Kwon, Hyung-Joo .
CANCER RESEARCH, 2014, 74 (14) :3844-3856
[48]   Prevention and Therapy of Hepatocellular Carcinoma by Vaccination with TM4SF5 Epitope-CpG-DNA-Liposome Complex without Carriers [J].
Kwon, Sanghoon ;
Kim, Dongbum ;
Park, Byoung Kwon ;
Cho, Sunhee ;
Kim, Kwang Dong ;
Kim, Young-Eun ;
Park, Cheung-Seog ;
Ahn, Hyun-Jong ;
Seo, Jae-Nam ;
Choi, Kyung-Chan ;
Kim, Doo-Sik ;
Lee, Younghee ;
Kwon, Hyung-Joo .
PLOS ONE, 2012, 7 (03)
[49]   Tetraspanin TM4SF5 mediates loss of contact inhibition through epithelial-mesenchymal transition in human hepatocarcinoma [J].
Lee, Sin-Ae ;
Lee, Sung-Yul ;
Cho, Ik-Hyun ;
Oh, Min-A ;
Kang, Eun-Sil ;
Kim, Yong-Bae ;
Seo, Woo Duck ;
Choi, Suyong ;
Nam, Ju-Ock ;
Tamamori-Adachi, Mimi ;
Kitajima, Shigetaka ;
Ye, Sang-Kyu ;
Kim, Semi ;
Hwang, Yoon-Jin ;
Kim, In-San ;
Park, Ki Hun ;
Lee, Jung Weon .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (04) :1354-1366
[50]   Blockade of Four-Transmembrane L6 Family Member 5 (TM4SF5)-Mediated Tumorigenicity in Hepatocytes by a Synthetic Chalcone Derivative [J].
Lee, Sin-Ae ;
Ryu, Hyung Won ;
Kim, Young Mee ;
Choi, Suyong ;
Lee, Mi Ji ;
Kwak, Tae Kyoung ;
Kim, Hyeon Jung ;
Cho, Moonjae ;
Park, Ki Hun ;
Lee, Jung Weon .
HEPATOLOGY, 2009, 49 (04) :1316-1325