2016
DOI: 10.1016/j.gore.2016.09.004
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Epithelial ovarian cancer inherent resistance: May the pleiotropic interaction between reduced immunosurveillance and drug-resistant cells play a key role?

Abstract: HighlightsCancer cells may have inherent chemoresistance which allows an indefinite expansion.Transformed ovarian epithelial cells may undergo an immunoediting process.Immunoedited ovarian cancer drug-resistant cells escape first-line chemotherapy.

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Cited by 51 publications
(30 citation statements)
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“…Recurrant oviarian cancer typically poorly responds to first, and sometimes even second line chemotherapy. In this scenario, it possible that the ovarian cancer inherent resistance may be due to reduced immunosurveillance and drugresistant cells [18,19]. Surgical removal of drug-resistant tumors can obtain the maximum clinical benefit.…”
Section: Discussionmentioning
confidence: 99%
“…Recurrant oviarian cancer typically poorly responds to first, and sometimes even second line chemotherapy. In this scenario, it possible that the ovarian cancer inherent resistance may be due to reduced immunosurveillance and drugresistant cells [18,19]. Surgical removal of drug-resistant tumors can obtain the maximum clinical benefit.…”
Section: Discussionmentioning
confidence: 99%
“…Cancer cell drug-resistance mechanisms play a critical role [34,35]. A growing notion is that reduced immune surveillance and immune escape also plays a crucial role in cancer progression [36,37]. Yet, evidence suggests that certain types of chemotherapy may in fact reboost tumor immune response by inducing immunogenic cell death [20].…”
Section: Discussionmentioning
confidence: 99%
“…The combination of younger age, AVB, and nulliparity, as well as other characteristics, including obesity, in women with synchronous endometrioid/endometrial carcinomas suggests the involvement of a hormonal “field effect” in the development of these simultaneous tumors, particularly endometrioid cell-type tumors [ 14 , 19 ]. In recent years, accumulating evidence has suggested that ovarian cancer arises from the pleiotropic interactions of the committed stem cells within the ovary, the surrounding microenvironment, and the infiltrating immune cells [ 20 , 21 ]. Thus, whether these interactions may contribute to the development of synchronous endometrial and ovarian disorders needs further exploration.…”
Section: Discussionmentioning
confidence: 99%