Abstract

ObjectivesThe aim of this study was to identify tumor-derived DNA from Papanicolaou (Pap) smear and plasma specimens collected from patients with endometrial cancer or atypical hyperplasia (EC/AH) or epithelial ovarian cancer (OC).MethodsTumor tissues, peripheral blood, and Pap smear samples were collected from patients with EC/AH and patients with epithelial OC. Somatic mutations of tumor specimens in EC/AH and OC were examined by whole-exome sequencing using a 127-driver gene panel from The Cancer Genome Atlas (TCGA). A nine-gene EC/AH panel and an eight-gene OC panel were established based on the identified significantly mutated genes in the EC/AH and OC tumor specimens. Circulating single-molecule amplification and resequencing technology (cSMART) was applied to evaluate somatic mutations in Pap smear DNA and plasma circulating cell-free DNA (ccfDNA) using the EC/AH and OC gene panels.ResultsIn EC/AH group, there existed 22 tumors and 14 of the 22 tumors contributed hot spot mutations for the EC/AH nine-gene panel. In the Pap smear subgroup, all 21 Pap smears tested positive. Nine out of 11 (81.8%) identified the same gene mutations with their matched tumors and the remaining 10 Pap smears all tested positive. In the plasma subgroup, 10 out of 26 (38.5%) plasmas tested positive. One out of 13 (7.7%) identified the same gene mutation with its matched tumor and 5 out of the remaining 13 plasmas (38.5%) tested positive. In OC group, there existed 17 tumors and 16 of the 17 tumors contributed hot spot mutations for the OC eight-gene panel. In the Pap smear subgroup, all 11 Pap smears tested positive. Five out of 10 (50.0%) identified the same gene mutations with their matched tumors and the remaining one Pap smear also tested positive. In the plasma subgroup, all 22 plasmas tested positive. Ten out of 14 (71.4%) identified the same gene mutation with their matched tumors and the remaining 4 plasmas all tested positive.ConclusionsTumor-derived DNA can be detected in Pap smears and plasmas from patients with EC/AH or epithelial OC. Using a small gene-panel, early detection of EC/AH and OC might be promising. However, the value of plasma ccfDNA for EC/AH requires further investigation.

Highlights

  • Among the tumors of the female reproductive tract, known as Mullerian duct tumors, epithelial ovarian cancer (OC) comprises the most intractable tumors with high rates

  • During the study period (November 2014–June 2015), there were 70 patients with suspected epithelial ovarian, fallopian tube or primary peritoneal cancer (OC), or endometrial cancer or atypical endometrial hyperplasia (EC or AH) at our clinic, who were fully informed of the risks and benefits of participating the study

  • Sixty-five of the 70 patients agreed to participate in the study if they had pathologically confirmed epithelial OC, EC, or AH

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Summary

Introduction

Among the tumors of the female reproductive tract, known as Mullerian duct tumors, epithelial ovarian cancer (OC) comprises the most intractable tumors with high rates. Epithelial OC is the leading cause of gynecologic cancer-related deaths in women, primarily because most patients present with advanced-stage disease. The 5-year survival rate remains at a low level [1, 2]. In the last 20 years, the incidence rate of endometrial cancer (EC) in the world has increased by 125%, and the death rate has increased by 65.2% [3, 4]. Despite improved diagnosis and treatment methods, up to 30% of EC patients are primarily diagnosed with stage III or IV EC and have poor outcomes. More techniques are needed for detecting these tumors at an early stage and helping improve the survival of these patients

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