BACKGROUND:Recent advances suggest fallopian tube as the main cellular source for women's pelvic serous carcinoma (PSC). In addition to TP53 mutations, many other genetic changes are involved in pelvic serous carcinogenesis. IMP3 is an oncofetal protein which has recently been observed to be overexpressed in benign-looking tubal epithelia. Such findings prompted us to examine the relationship between IMP3 over-expression, patient age and the likelihood of development of PSC.METHODS:Fallopian tubes from three groups (low-risk, high-risk, and PSC) of patients with matched ages were studied. Age was recorded in 10years intervals ranging from age 20 to older than 80. The number of IMP3 signatures (defined by 10 or more tubal secretory cells stained positively and continuously in benign appearing tubal mucosa) from both tubal fimbria and ampulla segments was measured. The data was analyzed by standard contingency table and Poisson distribution methods after age adjustment. IMP3 overexpression was also examined in serous tubal intraepithelial carcinoma and PSC.RESULTS:The positive IMP3-stained cells are mainly tubal secretory cells. The absolute number of tubal IMP3 signatures increased significantly within each age group. Age remained a significant risk factor for serous neoplasia after age adjustment. IMP3 signatures were more frequent in the patients of both high-risk and PSC groups. The presence of IMP3 signatures in tubal mucosa was significantly associated with tubal or pelvic serous carcinogenesis (p<0.001).CONCLUSIONS:The findings suggest that tubal secretory cells with IMP3 signatures showing growth advantage could potentially serve as a latent precancer biomarker for tubal or pelvic serous carcinomas in women.
| Identifer | oai:union.ndltd.org:arizona.edu/oai:arizona.openrepository.com:10150/610186 |
| Date | January 2014 |
| Creators | Wang, Yiying, Wang, Yue, Li, Dake, Li, Lingmin, Zhang, Wenjing, Yao, Guang, Jiang, Zhong, Zheng, Wenxin |
| Contributors | Department of Obstetrics and Gynecology, Henan Provincial People’s Hospital, Zhengzhou, China, Department of Pathology, University of Arizona College of Medicine, Tucson, AZ, USA, Department of Obstetrics and Gynecology, Jiangsu Provincial Hospital of Traditional Chinese Medicine, Nanjing, Jiangsu, China, Department of Pathology, Shanxi Medical University, Shanxi, China, Department of Obstetrics and Gynecology, Qilu Hospital, Shandong University, Jinan, Shandong, China, Arizona Cancer Center, University of Arizona, Tucson, AZ, USA, Department of Molecular & Cellular Biology, University of Arizona, Tucson, AZ, USA, Department of Obstetrics and Gynecology, University of Arizona, Tucson, AZ, USA, Department of Pathology, University of Massachusetts Medical Center, Worcester, MA, USA |
| Publisher | BioMed Central |
| Source Sets | University of Arizona |
| Language | English |
| Detected Language | English |
| Type | Article |
| Rights | © 2014 Wang et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) |
| Relation | http://www.jhoonline.org/content/7/1/49 |
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