Assessment of peritoneal microbial features and tumor marker levels as potential diagnostic tools for ovarian cancer
Epithelial ovarian cancer (OC) is the most deadly cancer of the female reproductive system. To date, there is no effective screening method for early detection of OC and current diagnostic armamentarium may include sonographic grading of the tumor and analyzing serum levels of tumor markers, Cancer...
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| Published in | PloS one Vol. 15; no. 1; p. e0227707 |
|---|---|
| Main Authors | , , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Public Library of Science
09.01.2020
Public Library of Science (PLoS) |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1932-6203 1932-6203 |
| DOI | 10.1371/journal.pone.0227707 |
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| Abstract | Epithelial ovarian cancer (OC) is the most deadly cancer of the female reproductive system. To date, there is no effective screening method for early detection of OC and current diagnostic armamentarium may include sonographic grading of the tumor and analyzing serum levels of tumor markers, Cancer Antigen 125 (CA-125) and Human epididymis protein 4 (HE4). Microorganisms (bacterial, archaeal, and fungal cells) residing in mucosal tissues including the gastrointestinal and urogenital tracts can be altered by different disease states, and these shifts in microbial dynamics may help to diagnose disease states. We hypothesized that the peritoneal microbial environment was altered in patients with OC and that inclusion of selected peritoneal microbial features with current clinical features into prediction analyses will improve detection accuracy of patients with OC. Blood and peritoneal fluid were collected from consented patients that had sonography confirmed adnexal masses and were being seen at SIU School of Medicine Simmons Cancer Institute. Blood was processed and serum HE4 and CA-125 were measured. Peritoneal fluid was collected at the time of surgery and processed for Next Generation Sequencing (NGS) using 16S V4 exon bacterial primers and bioinformatics analyses. We found that patients with OC had a unique peritoneal microbial profile compared to patients with a benign mass. Using ensemble modeling and machine learning pathways, we identified 18 microbial features that were highly specific to OC pathology. Prediction analyses confirmed that inclusion of microbial features with serum tumor marker levels and control features (patient age and BMI) improved diagnostic accuracy compared to currently used models. We conclude that OC pathogenesis alters the peritoneal microbial environment and that these unique microbial features are important for accurate diagnosis of OC. Our study warrants further analyses of the importance of microbial features in regards to oncological diagnostics and possible prognostic and interventional medicine. |
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| AbstractList | Epithelial ovarian cancer (OC) is the most deadly cancer of the female reproductive system. To date, there is no effective screening method for early detection of OC and current diagnostic armamentarium may include sonographic grading of the tumor and analyzing serum levels of tumor markers, Cancer Antigen 125 (CA-125) and Human epididymis protein 4 (HE4). Microorganisms (bacterial, archaeal, and fungal cells) residing in mucosal tissues including the gastrointestinal and urogenital tracts can be altered by different disease states, and these shifts in microbial dynamics may help to diagnose disease states. We hypothesized that the peritoneal microbial environment was altered in patients with OC and that inclusion of selected peritoneal microbial features with current clinical features into prediction analyses will improve detection accuracy of patients with OC. Blood and peritoneal fluid were collected from consented patients that had sonography confirmed adnexal masses and were being seen at SIU School of Medicine Simmons Cancer Institute. Blood was processed and serum HE4 and CA-125 were measured. Peritoneal fluid was collected at the time of surgery and processed for Next Generation Sequencing (NGS) using 16S V4 exon bacterial primers and bioinformatics analyses. We found that patients with OC had a unique peritoneal microbial profile compared to patients with a benign mass. Using ensemble modeling and machine learning pathways, we identified 18 microbial features that were highly specific to OC pathology. Prediction analyses confirmed that inclusion of microbial features with serum tumor marker levels and control features (patient age and BMI) improved diagnostic accuracy compared to currently used models. We conclude that OC pathogenesis alters the peritoneal microbial environment and that these unique microbial features are important for accurate diagnosis of OC. Our study warrants further analyses of the importance of microbial features in regards to oncological diagnostics and possible prognostic and interventional medicine. Epithelial ovarian cancer (OC) is the most deadly cancer of the female reproductive system. To date, there is no effective screening method for early detection of OC and current diagnostic armamentarium may include sonographic grading of the tumor and analyzing serum levels of tumor markers, Cancer Antigen 125 (CA-125) and Human epididymis protein 4 (HE4). Microorganisms (bacterial, archaeal, and fungal cells) residing in mucosal tissues including the gastrointestinal and urogenital tracts can be altered by different disease states, and these shifts in microbial dynamics may help to diagnose disease states. We hypothesized that the peritoneal microbial environment was altered in patients with OC and that inclusion of selected peritoneal microbial features with current clinical features into prediction analyses will improve detection accuracy of patients with OC. Blood and peritoneal fluid were collected from consented patients that had sonography confirmed adnexal masses and were being seen at SIU School of Medicine Simmons Cancer Institute. Blood was processed and serum HE4 and CA-125 were measured. Peritoneal fluid was collected at the time of surgery and processed for Next Generation Sequencing (NGS) using 16S V4 exon bacterial primers and bioinformatics analyses. We found that patients with OC had a unique peritoneal microbial profile compared to patients with a benign mass. Using ensemble modeling and machine learning pathways, we identified 18 microbial features that were highly specific to OC pathology. Prediction analyses confirmed that inclusion of microbial features with serum tumor marker levels and control features (patient age and BMI) improved diagnostic accuracy compared to currently used models. We conclude that OC pathogenesis alters the peritoneal microbial environment and that these unique microbial features are important for accurate diagnosis of OC. Our study warrants further analyses of the importance of microbial features in regards to oncological diagnostics and possible prognostic and interventional medicine.Epithelial ovarian cancer (OC) is the most deadly cancer of the female reproductive system. To date, there is no effective screening method for early detection of OC and current diagnostic armamentarium may include sonographic grading of the tumor and analyzing serum levels of tumor markers, Cancer Antigen 125 (CA-125) and Human epididymis protein 4 (HE4). Microorganisms (bacterial, archaeal, and fungal cells) residing in mucosal tissues including the gastrointestinal and urogenital tracts can be altered by different disease states, and these shifts in microbial dynamics may help to diagnose disease states. We hypothesized that the peritoneal microbial environment was altered in patients with OC and that inclusion of selected peritoneal microbial features with current clinical features into prediction analyses will improve detection accuracy of patients with OC. Blood and peritoneal fluid were collected from consented patients that had sonography confirmed adnexal masses and were being seen at SIU School of Medicine Simmons Cancer Institute. Blood was processed and serum HE4 and CA-125 were measured. Peritoneal fluid was collected at the time of surgery and processed for Next Generation Sequencing (NGS) using 16S V4 exon bacterial primers and bioinformatics analyses. We found that patients with OC had a unique peritoneal microbial profile compared to patients with a benign mass. Using ensemble modeling and machine learning pathways, we identified 18 microbial features that were highly specific to OC pathology. Prediction analyses confirmed that inclusion of microbial features with serum tumor marker levels and control features (patient age and BMI) improved diagnostic accuracy compared to currently used models. We conclude that OC pathogenesis alters the peritoneal microbial environment and that these unique microbial features are important for accurate diagnosis of OC. Our study warrants further analyses of the importance of microbial features in regards to oncological diagnostics and possible prognostic and interventional medicine. |
| Audience | Academic |
| Author | Martin, Jongjin Anne Ghareeb, Allen Badger, Taylor C. Braundmeier-Fleming, Andrea Auvil, Loretta Welge, Michael Brard, Laurent Zhu, Ruoqing Bushell, Colleen Diaz-Sylvester, Paula L. Miao, Ruizhong Groesch, Kathleen Cregger, Melissa Wilson, Teresa |
| AuthorAffiliation | 1 Department of Statistics, University of Virginia, Charlottesville, Virginia, United States of America 2 Department of Medical Microbiology, Immunology and Cell Biology, SIU School of Medicine, Springfield, Illinois, United States of America 5 Oak Ridge National Laboratory, Oak Ridge, Tennessee, United States of America 7 National Center for Supercomputing Applications, University of Illinois at Urbana-Champaign, Champaign, Illinois, United States of America 9 Department of Statistics, University of Illinois at Urbana-Champaign, Champaign, Illinois, United States of America 4 Department of Obstetrics & Gynecology, SIU School of Medicine, Springfield, Illinois, United States of America 3 Center for Clinical Research, SIU School of Medicine, Springfield, Illinois, United States of America 6 Department of Ecology and Evolutionary Biology, University of Tennessee, Knoxville, Tennessee, United States of America University of Insubria, ITALY 8 Applied Research Institute, University of Illinois at Ur |
| AuthorAffiliation_xml | – name: 8 Applied Research Institute, University of Illinois at Urbana-Champaign, Champaign, Illinois, United States of America – name: 9 Department of Statistics, University of Illinois at Urbana-Champaign, Champaign, Illinois, United States of America – name: 7 National Center for Supercomputing Applications, University of Illinois at Urbana-Champaign, Champaign, Illinois, United States of America – name: 5 Oak Ridge National Laboratory, Oak Ridge, Tennessee, United States of America – name: 3 Center for Clinical Research, SIU School of Medicine, Springfield, Illinois, United States of America – name: 4 Department of Obstetrics & Gynecology, SIU School of Medicine, Springfield, Illinois, United States of America – name: 2 Department of Medical Microbiology, Immunology and Cell Biology, SIU School of Medicine, Springfield, Illinois, United States of America – name: 1 Department of Statistics, University of Virginia, Charlottesville, Virginia, United States of America – name: 6 Department of Ecology and Evolutionary Biology, University of Tennessee, Knoxville, Tennessee, United States of America – name: University of Insubria, ITALY – name: 10 Simmons Cancer Institute at SIU, Springfield, Illinois, United States of America |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31917801$$D View this record in MEDLINE/PubMed https://www.osti.gov/biblio/1581861$$D View this record in Osti.gov |
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| Snippet | Epithelial ovarian cancer (OC) is the most deadly cancer of the female reproductive system. To date, there is no effective screening method for early detection... |
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| SubjectTerms | 60 APPLIED LIFE SCIENCES Aged Antigens Ascites Ascitic Fluid - microbiology Bioinformatics Biology Biology and Life Sciences Biomarkers Blood CA-125 Antigen - blood Cancer Cancer detection and diagnosis Cancer research Carcinoma, Ovarian Epithelial - blood Carcinoma, Ovarian Epithelial - diagnosis Carcinoma, Ovarian Epithelial - microbiology Carcinoma, Ovarian Epithelial - surgery Clostridium Computational biology Computer and Information Sciences Cross-Sectional Studies Development and progression Diagnostic imaging Diagnostic medicine Diagnostic software Diagnostic systems Disease DNA, Bacterial - genetics DNA, Bacterial - isolation & purification Epididymis Female Fungi Gynecology Health screening Humans Hysterectomy Immunology Laparoscopy Learning algorithms Machine Learning Markers Medical diagnosis Medical schools Medicine Medicine and Health Sciences Membrane Proteins - blood Microbiome Microbiota - genetics Microorganisms Middle Aged Model accuracy Models, Biological Mucosa Next-generation sequencing Obstetrics Ovarian cancer Ovarian carcinoma Ovarian Neoplasms - blood Ovarian Neoplasms - diagnosis Ovarian Neoplasms - microbiology Ovarian Neoplasms - surgery Ovariectomy Pathogenesis Patients Peritoneal fluid Peritoneum Pilot Projects Preoperative Period Prognosis Reproductive system RNA, Ribosomal, 16S - genetics Serum levels Surgery Surgical oncology Tumor markers Tumors Ultrasonic imaging Ultrasound imaging WAP Four-Disulfide Core Domain Protein 2 - analysis Womens health |
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| Title | Assessment of peritoneal microbial features and tumor marker levels as potential diagnostic tools for ovarian cancer |
| URI | https://www.ncbi.nlm.nih.gov/pubmed/31917801 https://www.proquest.com/docview/2335077649 https://www.proquest.com/docview/2336254691 https://www.osti.gov/biblio/1581861 https://pubmed.ncbi.nlm.nih.gov/PMC6952086 https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0227707&type=printable https://doaj.org/article/2f9429bdc7964d1695a50621cbb6904a http://dx.doi.org/10.1371/journal.pone.0227707 |
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