Human Papilloma viruses and Breast Cancer - Assessment of Causality

被引:22
作者
Lawson, James Sutherland [1 ]
Glenn, Wendy K. [1 ]
Whitaker, Noel James [1 ]
机构
[1] Univ New South Wales, Sch BABS, Sydney, NSW, Australia
来源
FRONTIERS IN ONCOLOGY | 2016年 / 6卷
关键词
breast cancer; human papilloma virus; HPV; causality; RISK HUMAN PAPILLOMAVIRUSES; EPSTEIN-BARR-VIRUS; IN-SITU; HPV; ASSOCIATION; DNA; PREVALENCE; EXPRESSION; INFECTION; WOMEN;
D O I
10.3389/fonc.2016.00207
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
High risk human papilloma viruses (HPVs) may have a causal role in some breast cancers. Case-control studies, conducted in many different countries, consistently indicate that HPVs are more frequently present in breast cancers as compared to benign breast and normal breast controls (odds ratio 4.02). The assessment of causality of HPVs in breast cancer is difficult because (i) the HPV viral load is extremely low, (ii) HPV infections are common but HPV associated breast cancers are uncommon, and (iii) HPV infections may precede the development of breast and other cancers by years or even decades. Further, HPV oncogenesis can be indirect. Despite these difficulties, the emergence of new evidence has made the assessment of HPV causality, in breast cancer, a practical proposition. With one exception, the evidence meets all the conventional criteria for a causal role of HPVs in breast cancer. The exception is "specificity." HPVs are ubiquitous, which is the exact opposite of specificity. An additional reservation is that the prevalence of breast cancer is not increased in immunocompromised patients as is the case with respect to HPV-associated cervical cancer. This indicates that HPVs may have an indirect causal influence in breast cancer. Based on the overall evidence, high-risk HPVs may have a causal role in some breast cancers.
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页数:7
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共 58 条
[51]   Investigation of Human Cancers for Retrovirus by Low-Stringency Target Enrichment and High-Throughput Sequencing [J].
Vinner, Lasse ;
Mourier, Tobias ;
Friis-Nielsen, Jens ;
Gniadecki, Robert ;
Dybkaer, Karen ;
Rosenberg, Jacob ;
Langhoff, Jill Levin ;
Cruz, David Flores Santa ;
Fonager, Jannik ;
Izarzugaza, Jose M. G. ;
Gupta, Ramneek ;
Sicheritz-Ponten, Thomas ;
Brunak, Soren ;
Willerslev, Eske ;
Nielsen, Lars Peter ;
Hansen, Anders Johannes .
SCIENTIFIC REPORTS, 2015, 5
[52]   Causality in medicine: the case of tumours and viruses [J].
Vonka, V .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2000, 355 (1404) :1831-1841
[53]   IMMORTALIZATION OF DISTINCT HUMAN MAMMARY EPITHELIAL-CELL TYPES BY HUMAN PAPILLOMA-VIRUS-16 E6 OR E7 [J].
WAZER, DE ;
LIU, XL ;
CHU, QM ;
GAO, QS ;
BAND, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (09) :3687-3691
[54]  
World Health Organisation, 2015, GLOBOCAN 2012
[55]   E6/E7 of HPV type 16 promotes cell invasion and metastasis of human breast cancer cells [J].
Yasmeen, Amber ;
Bismar, Tarek A. ;
Kandouz, Mustapha ;
Foulkes, William D. ;
Desprez, Pierre-Yves ;
Al Moustafa, Ala-Eddin .
CELL CYCLE, 2007, 6 (16) :2038-2042
[56]  
Yu YY, 1999, ANTICANCER RES, V19, P5057
[57]   Inconclusive role of human papillomavirus infection in breast cancer [J].
Zhou, Yi ;
Li, Jinyuan ;
Ji, Yuting ;
Ren, Ming ;
Pang, Bo ;
Chu, Ming ;
Wei, Lanlan .
INFECTIOUS AGENTS AND CANCER, 2015, 10
[58]   Papillomaviruses and cancer: From basic studies to clinical application [J].
zur Hausen, H .
NATURE REVIEWS CANCER, 2002, 2 (05) :342-350