Abstract

Simple SummaryAll cells have a complex internal network of ‘communication chains’ called signal transduction pathways (STPs). Through interaction of different proteins in STPs, they are partly responsible for the behavior of a cell. In our study, we investigated the activity of six STPs in 85 women with advanced stage high-grade serous ovarian cancer (HGSC). To investigate the relation between and differences in survival and STP activity, women with a short disease-free survival (below 12 months) and a long disease-free survival (above 24 months) were included. We found no differences in mean STP activity between short-term survivors (52 women) and long-term survivors (33 women). However, when we analyzed postmenopausal women, we found that both disease-free and overall survival were related to estrogen receptor (ER) pathway signaling. This indicates that a better survival outcome was related to a more active ER pathway in this subgroup.High-grade serous ovarian carcinoma (HGSC), the most common subtype of ovarian cancer, has a high mortality rate. Although there are some factors associated with survival, such as stage of disease, there are remarkable differences in survival among women diagnosed with advanced stage disease. In this study, we investigate possible relations between survival and signal transduction pathway (STP) activity. We assessed the functional activity of the androgen receptor (AR), estrogen receptor (ER), phosphoinositide-3-kinase (PI3K), Hedgehog (HH), transforming growth factor beta (TGF-β) and canonical wingless-type MMTV integration site (Wnt) pathway in 85 primary tumor samples of patients with FIGO stage IIIC to IVB HGSC and disease-free survival (DFS) below 12 (n = 52) or over 24 months (n = 33). There were no significant differences in median pathway activity between patients with a short and long DFS. In univariate Cox proportional hazards analysis, ER pathway activity was related to a favorable DFS and overall survival (OS) in postmenopausal women (p = 0.033 and p = 0.041, respectively), but not in premenopausal women. We divided the postmenopausal group into subgroups based on ER pathway activity quartiles. Survival analysis revealed that postmenopausal women in the lowest ER quartile had a shorter DFS and OS (log-rank p = 0.006 and p < 0.001, respectively). Furthermore, we were able to form subgroups of patients based on an inverse relation between ER and PI3K pathway activity. In conclusion, in postmenopausal patients with advanced stage HGSC, a poorer survival outcome was associated with low functional ER pathway activity.

Highlights

  • Ovarian cancer is the most lethal gynecological malignancy and the fifth leading cause of cancer related death in women [1]

  • We identified 580 patients with advanced stage High-grade serous ovarian carcinoma (HGSC) in the NCR database treated in our region, 157 of which met our eligibility criteria

  • signal transduction pathway (STP) activity results of 85 patients were included in our analysis, of which 52 were in the short disease-free survival (DFS) group and 33 in the long DFS group

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Summary

Introduction

Ovarian cancer is the most lethal gynecological malignancy and the fifth leading cause of cancer related death in women [1]. High-grade serous ovarian carcinoma (HGSC) is the most common histotype of ovarian cancer and is often detected at an advanced stage of disease (i.e., FIGO stage IIIC-IVB) [2,3] At this point, the overall five-year survival rate is less than 40%, even after successful first-line treatment with debulking surgery and chemotherapy [2]. Several clinicopathological factors associated with improved survival have been established like stage of disease, CA125 concentration at diagnosis and after treatment, the possibility of primary debulking surgery and residual disease after surgery. Immune factors such as tumor infiltrating lymphocytes have been identified as prognostic factors [5,6]. Research aimed at the analysis of gene expression profiles and patterns to reveal a relation to survival, could not confirm this for ovarian carcinoma [7]

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