HCC heterogeneity: Molecular pathogenesis and clinical implications

被引:34
作者
Fransvea, Emilia [1 ]
Paradiso, Angelo [2 ]
Antonaci, Salvatore [1 ]
Giannelli, Gianluigi [1 ]
机构
[1] Univ Bari, Dept Internal Med Immunol & Infect Dis, Sect Internal Med, Sch Med, I-70124 Bari, Italy
[2] Natl Canc Inst, Clin Expt Oncol Lab, Bari, Italy
关键词
Biological therapies; HCC; molecular pathogenesis; TGF-beta; 1; tissue microenvironment; TK-receptors; tumor progression; heterogeneity; HUMAN HEPATOCELLULAR-CARCINOMA; GROWTH-FACTOR-BETA; CELL LUNG-CANCER; EPITHELIAL-MESENCHYMAL TRANSITIONS; E-CADHERIN; TGF-BETA; PHASE-II; MATRIX METALLOPROTEINASES; COLORECTAL-CANCER; TUMOR PROGRESSION;
D O I
10.3233/CLO-2009-0473
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Hepatocellular carcinoma (HCC) poses a major challenge because of the extreme variability of the clinical outcome, which makes it difficult to properly stage the disease and thereby estimate the prognosis. There is growing evidence that this heterogeneous clinical behavior is attributable to several different biological pathways. A novel approach to mapping these differences is by investigating the epigenetics associated with certain clinical aspects. Design: Herein, the relevance of these molecular differences in combination with the biological and molecular pathways regulating the clinical outcome will be discussed. Use of a mechanistic and pathogenic approach to clarify the natural history of HCC is not just an academic speculation but should help to develop new therapies and to tailor these therapies to each individual patient. Conclusion: New biological therapies targeting components of the tumoral or peritumoral microenvironment are crucial to the fight against HCC. However, biological redundancies and the presence of several growth factors, hormones, cytokines, etc., potentially involved in HCC tumor progression make it difficult to assess the best target. Sorafenib, a multi-tyrosine kinase inhibitor, blocks the functions of different growth factors present in the tissue microenvironment. The use of Sorafenib in patients with HCC offers a new approach to the therapy of this disease, stimulating research focusing on the development of drugs based on new molecular and pathogenic insights.
引用
收藏
页码:227 / 233
页数:7
相关论文
共 57 条
[1]   Phase II study of sorafenib in patients with advanced hepatocellular carcinoma [J].
Abou-Alfa, Ghassan K. ;
Schwartz, Lawrence ;
Ricci, Sergio ;
Amadori, Dino ;
Santoro, Armando ;
Figer, Arie ;
De Greve, Jacques ;
Douillard, Jean-Yves ;
Lathia, Chetan ;
Schwartz, Brian ;
Taylor, Ian ;
Moscovici, Marius ;
Saltz, Leonard B. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (26) :4293-4300
[2]   TRANSFORMING GROWTH-FACTOR-BETA-1 (TGF-BETA-1) AND TGF-BETA-1 RECEPTORS IN NORMAL, CIRRHOTIC, AND NEOPLASTIC HUMAN LIVERS [J].
BEDOSSA, P ;
PELTIER, E ;
TERRIS, B ;
FRANCO, D ;
POYNARD, T .
HEPATOLOGY, 1995, 21 (03) :760-766
[3]   Laminin-5 stimulates hepatocellular carcinoma growth through a different function of α6β4 and α3β1 integrins [J].
Bergamini, Carlo ;
Sgarra, Concetta ;
Trerotoli, Paolo ;
Lupo, Luigi ;
Azzariti, Amalia ;
Antonaci, Salvatore ;
Giannelli, Gianluigi .
HEPATOLOGY, 2007, 46 (06) :1801-1809
[4]   Invasion and metastasis in colorectal cancer:: Epithelial-mesenchymal transition, mesenchymal-epithelial transition, stem cells and β-catenin [J].
Brabletz, T ;
Hlubek, F ;
Spaderna, S ;
Schmalhofer, O ;
Hiendlmeyer, E ;
Jung, A ;
Kirchner, T .
CELLS TISSUES ORGANS, 2005, 179 (1-2) :56-65
[5]   Dysregulation of growth factor signaling in human hepatocellular carcinoma [J].
Breuhahn, K. ;
Longerich, T. ;
Schirmacher, P. .
ONCOGENE, 2006, 25 (27) :3787-3800
[6]   Management of hepatoceullular carcinoma [J].
Bruix, J ;
Sherman, M .
HEPATOLOGY, 2005, 42 (05) :1208-1236
[7]   A NEW NOMENCLATURE FOR THE LAMININS [J].
BURGESON, RE ;
CHIQUET, M ;
DEUTZMANN, R ;
EKBLOM, P ;
ENGEL, J ;
KLEINMAN, H ;
MARTIN, GR ;
MENEGUZZI, G ;
PAULSSON, M ;
SANES, J ;
TIMPL, R ;
TRYGGVASON, K ;
YAMADA, Y ;
YURCHENCO, PD .
MATRIX BIOLOGY, 1994, 14 (03) :209-211
[8]   The transcription factor Snail controls epithelial-mesenchymal transitions by repressing E-cadherin expression [J].
Cano, A ;
Pérez-Moreno, MA ;
Rodrigo, I ;
Locascio, A ;
Blanco, MJ ;
del Barrio, MG ;
Portillo, F ;
Nieto, MA .
NATURE CELL BIOLOGY, 2000, 2 (02) :76-83
[9]   Natural history and pathogenesis of hepatitis C virus related hepatocellular carcinoma [J].
Colombo, M .
JOURNAL OF HEPATOLOGY, 1999, 31 :25-30
[10]   Development of ZD1839 in colorectal cancer [J].
Douglass, EC .
SEMINARS IN ONCOLOGY, 2003, 30 (03) :17-22