Abstract

Endometriosis is an inflammatory disease characterized by the presence of endometrium-like tissue outside the uterus primarily on pelvic organs and tissues. It affects up to 15% of women in the reproductive age group and is often associated with pelvic pain and subfertility. Different theories explain how retrograde menstruation gives rise to endometrial deposits at ectopic sites, and how several other factors are involved in the progression of the disease. Its final diagnosis is established through direct visualization at laparoscopy or surgery followed by histological confirmation. Available epidemiological reports along with histopathological observations and molecular studies shed interesting light on the pathogenetic basis of different variants of the disease like deep infiltrating endometriosis and ovarian endometriosis. Evidence also suggests that endometriosis is a neoplastic condition which serves as a precursor of ovarian and endometrial cancers. In the present review, we have attempted to take a stock of the current epidemiological and molecular knowledge regarding endometriosis associated cancers and develop a model of functional network with interactions among critical genomic factors regulating cellular processes leading to fibrotic reaction. It is being conjectured that cyclic bleeding associated with inflammatory and oxidative stress followed by repeated tissue injury and repair along with recurrent estrogenic stimulation and ovulatory events in the pelvic environment bring about the complex phenotype of atypical endometriosis and associated neoplasm with a trade-off malignant transformation in high risk population. Finally, we have presented an algorithm for pre-emptive monitoring and management of endometriosis-associated cancers.

Highlights

  • Endometriosis is characterized by the presence of endometrial cells at ectopic sites, primarily on the pelvic peritoneum and pelvic organs

  • In a study of selected tumor suppressor and oncogenes in eutopic tissue (EE) and autologous ET lesions obtained from women with ovarian endometriosis, Laudanski et al [118] observed higher levels of oncogene AKT serine/threonine Kinase 1 (AKT1) and tumor suppressor gene product 4EBP1 mRNAs and their protein expressions in EE of women with endometriosis compared with control patients suggesting up-regulation of AKT1 and 4EBP1 in EE might be associated with the pathogenesis

  • Driver modules are the key components of biological pathways that are highly relevant to the pathophysiology of endometriosis as these regulate the underlying pathophysiological processes including cellular proliferation, cell survival, epithelialmesenchymal transition (EMT), and angiogenesis, which may lead to fibrosis

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Summary

Introduction

Endometriosis is characterized by the presence of endometrial cells at ectopic sites, primarily on the pelvic peritoneum and pelvic organs.

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