Lessons from BRCA: The Tubal Fimbria Emerges as an Origin for Pelvic Serous Cancer

被引:237
作者
Crum, Christopher P. [1 ]
Drapkin, Ronny [2 ]
Kindelberger, David [1 ]
Medeiros, Fabiola [1 ]
Miron, Alexander [3 ]
Lee, Yonghee [1 ]
机构
[1] Brigham & Womens Hosp, Dept Pathol, Div Womens & Perinatal Pathol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Div Med Oncol, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Div Canc Biol, Boston, MA 02115 USA
关键词
BRCA; Fallopian tube neoplasms; Fimbria; Ovarian neoplasms; p53; SEE-FIM; Serous carcinoma;
D O I
10.3121/cmr.2007.702
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ovarian epithelial cancer is diagnosed in approximately 25,000 women yearly in the United States, accounting for approximately 12,500 deaths. Of these tumors, serous cancer is the most lethal, due to its capacity to spread beyond the reproductive tract and involve the peritoneal surfaces or distant organs. Conventional classification systems designate tumor origins principally on the location of the largest tumor. However, despite the fact that the largest tumors typically involve the ovaries, demonstrations of a precise starting point for these tumors, including precursor lesions, have been inconsistent. In recent years, a major effort to prevent serous cancer in genetically susceptible women with mutations in BRCA1 or BRCA2 has spawned the practice of prophylactic salpingo-oophorectomy. This practice has surprisingly revealed that many early cancers in these women arise in the fallopian tube, and further studies have pinpointed the distal (fimbrial) portion as the most common site of origin. Emerging studies that carefully examine the fallopian tubes suggest a high frequency of early cancer in the fimbria in unselected women with ovarian and peritoneal serous carcinoma, raising the distinct possibility that a significant proportion of these tumors have a fimbrial origin. The evidence for these discoveries and their relevance to serous cancer classification, early detection and prevention are addressed in this review. A model for pelvic serous cancer is proposed that takes into account five distinct variables which ultimately impact on origin and tumor distribution: (1) location of target epithelium, (2) genotoxic stress, (3) type of epithelium, (4) mitigating genetic factors, and (5) tumor spread pattern. Ultimately, this model illustrates the importance of identifying cancer precursors, inasmuch as these entities are useful as both surrogate endpoints for their respective malignancies in epidemiologic studies and natural targets for cancer prevention.
引用
收藏
页码:35 / 44
页数:10
相关论文
共 62 条
[1]   Unexpected gynecologic neoplasms in patients with proven or suspected BRCA-1 or-2 mutations - Implications for gross examination, cytology, and clinical follow-up [J].
Agoff, SN ;
Mendelin, JE ;
Grieco, VS ;
Garcia, RL .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2002, 26 (02) :171-178
[2]   Tumors of the fimbriated end of the Fallopian tube: A clinicopathologic analysis of 20 cases, including nine carcinomas [J].
AlvaradoCabrero, I ;
Navani, SS ;
Young, RH ;
Scully, RE .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 1997, 16 (03) :189-196
[3]  
Aoki Y, 2000, J REPROD MED, V45, P159
[4]   Intraperitoneal cisplatin and paclitaxel in ovarian cancer [J].
Armstrong, DK ;
Bundy, B ;
Wenzel, L ;
Huang, HQ ;
Baergen, R ;
Lele, S ;
Copeland, LJ ;
Walker, JL ;
Burger, RA .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (01) :34-43
[5]   A genetic epidemiological study of carcinoma of the fallopian tube [J].
Aziz, S ;
Kuperstein, G ;
Rosen, B ;
Cole, D ;
Nedelcu, R ;
McLaughlin, J ;
Narod, SA .
GYNECOLOGIC ONCOLOGY, 2001, 80 (03) :341-345
[6]  
BANNATYNE P, 1981, DIAGN GYNECOL OBSTET, V3, P49
[7]  
Barakat RR, 2000, CANCER, V89, P383, DOI 10.1002/1097-0142(20000715)89:2<383::AID-CNCR25>3.0.CO
[8]  
2-T
[9]   New tumor markers: CA125 and beyond [J].
Bast, RC ;
Badgwell, D ;
Lu, Z ;
Marquez, R ;
Rosen, D ;
Liu, J ;
Baggerly, KA ;
Atkinson, EN ;
Skates, S ;
Lokshin, A ;
Menon, U ;
Jacobs, I ;
Lu, K .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2005, 15 :274-281
[10]   Origins and molecular pathology of ovarian cancer [J].
Bell, DA .
MODERN PATHOLOGY, 2005, 18 :S19-S32