Non-viral causes of hepatocellular carcinoma

被引:169
作者
Blonski, Wojciech [1 ,2 ]
Kotlyar, David S. [3 ]
Forde, Kimberly A.
机构
[1] Univ Penn, Div Gastroenterol, Philadelphia, PA 19104 USA
[2] Med Univ, Dept Gastroenterol, PL-50556 Wroclaw, Poland
[3] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Internal Med, Bronx, NY 10467 USA
关键词
Hepatocellular carcinoma; Etiology; Non-alcoholic; steatohepatitis; Obesity; Diabetes; Alcohol; Tobacco; Oral contraceptive; ORAL-CONTRACEPTIVE USE; PRIMARY LIVER-CANCER; GAMMA-GLUTAMYL-TRANSFERASE; FOCAL NODULAR HYPERPLASIA; POPULATION-BASED COHORT; TUMOR-SUPPRESSOR GENE; AFRICAN IRON OVERLOAD; HEPATITIS-C VIRUS; UNITED-STATES; RISK-FACTORS;
D O I
10.3748/wjg.v16.i29.3603
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Hepatocellular carcinoma (HCC) is the most common primary liver malignancy and represents an international public health concern as one of the most deadly cancers worldwide. The main etiology of HCC is chronic infection with hepatitis B and hepatitis C viruses. However, there are other important factors that contribute to the international burden of HCC. Among these are obesity, diabetes, non-alcoholic steatohepatitis and dietary exposures. Emerging evidence suggests that the etiology of many cases of HCC is in fact multifactorial, encompassing infectious etiologies, comorbid conditions and environmental exposures. Clarification of relevant non-viral causes of HCC will aid in preventative efforts to curb the rising incidence of this disease. (C) 2010 Baishideng. All rights reserved.
引用
收藏
页码:3603 / 3615
页数:13
相关论文
共 117 条
[1]
The natural history of nonalcoholic fatty liver disease: A population-based cohort study [J].
Adams, LA ;
Lymp, JF ;
St Sauver, J ;
Sanderson, SO ;
Lindor, KD ;
Feldstein, A ;
Angulo, P .
GASTROENTEROLOGY, 2005, 129 (01) :113-121
[2]
AFLATOXIN-B(1) INDUCES THE TRANSVERSION OF G-]T IN CODON 249 OF THE P53 TUMOR-SUPPRESSOR GENE IN HUMAN HEPATOCYTES [J].
AGUILAR, F ;
HUSSAIN, SP ;
CERUTTI, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (18) :8586-8590
[3]
GEOGRAPHIC-VARIATION OF P53 MUTATIONAL PROFILE IN NONMALIGNANT HUMAN LIVER [J].
AGUILAR, F ;
HARRIS, CC ;
SUN, T ;
HOLLSTEIN, M ;
CERUTTI, P .
SCIENCE, 1994, 264 (5163) :1317-1319
[4]
Beutler E, 1997, AM J HUM GENET, V61, P762
[5]
CARCINOGENICITY OF BETEL QUID INGREDIENTS - FEEDING MICE WITH AQUEOUS EXTRACT AND THE POLYPHENOL FRACTION OF BETEL NUT [J].
BHIDE, SV ;
SHIVAPURKAR, NM ;
GOTHOSKAR, SV ;
RANADIVE, KJ .
BRITISH JOURNAL OF CANCER, 1979, 40 (06) :922-926
[6]
Increased incidence of HFE C282Y mutations in patients, with iron overload and hepatocellular carcinoma developed in non-cirrhotic liver [J].
Blanc, JF ;
De Ledinghen, V ;
Bernard, PH ;
de Verneuil, H ;
Winnock, M ;
Le Bail, B ;
Carles, J ;
Saric, J ;
Balabaud, C ;
Bioulac-Sage, P .
JOURNAL OF HEPATOLOGY, 2000, 32 (05) :805-811
[7]
Lack of association between HFE gene mutations and hepatocellular carcinoma in patients with cirrhosis [J].
Boige, V ;
Castéra, L ;
de Roux, N ;
Ganne-Carrié, N ;
Ducot, B ;
Pelletier, G ;
Beaugrand, M ;
Buffet, C .
GUT, 2003, 52 (08) :1178-1181
[8]
Hepatocellular carcinoma in the thalassaemia syndromes [J].
Borgna-Pignatti, C ;
Vergine, G ;
Lombardo, T ;
Cappellini, MD ;
Cianciulli, P ;
Maggio, A ;
Renda, D ;
Lai, ME ;
Mandas, A ;
Forni, G ;
Piga, A ;
Bisconte, MG .
BRITISH JOURNAL OF HAEMATOLOGY, 2004, 124 (01) :114-117
[9]
BRADBEAR RA, 1985, JNCI-J NATL CANCER I, V75, P81
[10]
Coffee drinking and hepatocellular carcinoma risk: A meta-analysis [J].
Bravi, Francesca ;
Bosetti, Cristina ;
Tavani, Alessandra ;
Bagnardi, Vincenzo ;
Gallus, Silvano ;
Negri, Eva ;
Franceschi, Silvia ;
La Vecchia, Carlo .
HEPATOLOGY, 2007, 46 (02) :430-435