Cause, Screening and Diagnosis in Ovarian Cancer

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Cancer Causes, Screening and Diagnosis".

Deadline for manuscript submissions: closed (31 October 2021) | Viewed by 5775

Special Issue Editors


E-Mail Website
Guest Editor
Stephenson Cancer Center, Oklahoma University Health Science Center, Oklahoma, OK 73104, USA
Interests: cancer; cell signaling; non-coding RNA; tumor microenvironment
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
Keio University School of Medicine, Tokyo, Japan

E-Mail Website
Guest Editor
Ottawa Hospital Research Institute, Ottawa, Canada
Interests: Human Ovarian Cancer Biology and Chemoresistance

E-Mail Website
Guest Editor
1. Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul 03080, Republic of Korea
2. Cancer Research Institute, Seoul National University College of Medicine, Seoul 03080, Republic of Korea
Interests: anti-cancer drugs discovery; tumor microenvironment; cell-to-cell communication; translational medicine in cancer; gynecologic oncology; phytochemical; diagnostic and prognostic biomarkers of cancer

Special Issue Information

Dear Colleagues,

Epithelial ovarian cancer is an uncommon pathology but is considered the main cause of death related to malignant gynecological cancer in women. Its particularity is based on its silent character responsible for a late diagnosis and therapeutic difficulty, especially in its extended forms. It has been called the "silent killer" because researchers once thought it is asymptomatic in the early stages of the disease, although it can now normally be diagnosed in the early stages either by imaging or by blood biomarkers. However, the expansion of ovarian cancer in the peritoneal cavity is unknown.

The aim of this Special Issue is to accumulate new results on different aspects of ovarian cancer, ovarian germ cell tumors, and Fallopian tube cancer, including their expansion in the peritoneal cavity, causes, biomarkers, screening, genetic anomalies, animal models, social impact, and diagnosis.

Prof. Dr. Danny N. Dhanasekaran
Prof. Daisuke A. Aoki
Dr. Benjamin Tsang
Prof. Dr. Yong Sang Song
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Cancers is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2900 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • deep learning model development
  • cancer genomics
  • tumor microenvironment
  • anticancer therapy
  • biomarker development
  • BRCA1/2
  • cancer genome profiling
  • drug sensitivity test

Published Papers (2 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Research

Jump to: Review

18 pages, 1559 KiB  
Article
Plasma Protein Biomarkers Associated with Higher Ovarian Cancer Risk in BRCA1/2 Carriers
by Hee-Sung Ahn, Jung Yoon Ho, Jiyoung Yu, Jeonghun Yeom, Sanha Lee, Soo Young Hur, Yuyeon Jung, Kyunggon Kim and Youn Jin Choi
Cancers 2021, 13(10), 2300; https://doi.org/10.3390/cancers13102300 - 11 May 2021
Cited by 6 | Viewed by 2500
Abstract
Ovarian cancer (OC) is the most lethal gynecologic malignancy and in-time diagnosis is limited because of the absence of effective biomarkers. Germline BRCA1/2 genetic alterations are risk factors for hereditary OC; risk-reducing salpingo-oophorectomy (RRSO) is pursued for disease prevention. However, not all healthy [...] Read more.
Ovarian cancer (OC) is the most lethal gynecologic malignancy and in-time diagnosis is limited because of the absence of effective biomarkers. Germline BRCA1/2 genetic alterations are risk factors for hereditary OC; risk-reducing salpingo-oophorectomy (RRSO) is pursued for disease prevention. However, not all healthy carriers develop the disease. Therefore, identifying predictive markers in the BRCA1/2 carrier population could help improve the identification of candidates for preventive RRSO. In this study, plasma samples from 20 OC patients (10 patients with BRCA1/2 wild type (wt) and 10 with the BRCA1/2 variant (var)) and 20 normal subjects (10 subjects with BRCA1/2wt and 10 with BRCA1/2var) were analyzed for potential biomarkers of hereditary OC. We applied a bottom-up proteomics approach, using nano-flow LC-MS to analyze depleted plasma proteome quantitatively, and potential plasma protein markers specific to the BRCA1/2 variant were identified from a comparative statistical analysis of the four groups. We obtained 1505 protein candidates from the 40 subjects, and SPARC and THBS1 were verified by enzyme-linked immunosorbent assay. Plasma SPARC and THBS1 concentrations in healthy BRCA1/2 carriers were found to be lower than in OC patients with BRCA1/2var. If plasma SPARC concentrations increase over 337.35 ng/mL or plasma THBS1 concentrations increase over 65.28 μg/mL in a healthy BRCA1/2 carrier, oophorectomy may be suggested. Full article
(This article belongs to the Special Issue Cause, Screening and Diagnosis in Ovarian Cancer)
Show Figures

Figure 1

Review

Jump to: Research

23 pages, 2453 KiB  
Review
Characteristics of Selected Adipokines in Ascites and Blood of Ovarian Cancer Patients
by Marcin Wróblewski, Karolina Szewczyk-Golec, Iga Hołyńska-Iwan, Joanna Wróblewska and Alina Woźniak
Cancers 2021, 13(18), 4702; https://doi.org/10.3390/cancers13184702 - 20 Sep 2021
Cited by 7 | Viewed by 2531
Abstract
Ovarian cancer is one of the most common malignancies among women worldwide. The course of the disease is often latent and asymptomatic in the early stages, but as it develops, metastasis occurs, accompanied by accumulation of ascites in the peritoneal cavity. The ascites [...] Read more.
Ovarian cancer is one of the most common malignancies among women worldwide. The course of the disease is often latent and asymptomatic in the early stages, but as it develops, metastasis occurs, accompanied by accumulation of ascites in the peritoneal cavity. The ascites fluid constitutes a specific microenvironment influencing the processes of carcinogenesis. In ascites, signaling is mediated by various cytokines that control tumor cell proliferation, progression, metastasis, and chemoresistance. Adipokines, secreted into ascites and also appearing in blood, may be markers of ongoing processes related to the development of neoplastic disease. Moreover, a significant influence of adipocyte lipids on the growth of tumors, for which they are one of energy sources, is observed. Adiponectin, interleukin 6 (IL-6), interleukin 8 (IL-8), monocyte chemotactic protein-1 (MCP-1) and tissue inhibitor of metalloproteinase-1 (TIMP-1), discussed in the present review, were found to mediate the effects of omentum metastasis through homing, migration and invasion of ovarian cancer cells. Further research on those adipokines seem to be a natural consequence, allowing for a better understanding of the mechanisms of neoplastic disease and determination of the treatment procedure. Full article
(This article belongs to the Special Issue Cause, Screening and Diagnosis in Ovarian Cancer)
Show Figures

Figure 1

Back to TopTop