Literature DB >> 26892153

Morphologic, Immunophenotypic, and Molecular Features of Epithelial Ovarian Cancer.

Preetha Ramalingam.   

Abstract

Epithelial ovarian cancer comprises a heterogeneous group of tumors. The four most common subtypes are serous, endometrioid, clear cell, and mucinous carcinoma. Less common are transitional cell tumors, including transitional cell carcinoma and malignant Brenner tumor. While in the past these subtypes were grouped together and designated as epithelial ovarian tumors, these tumor types are now known to be separate entities with distinct clinical and biologic behaviors. From a therapeutic standpoint, current regimens employ standard chemotherapy based on stage and grade rather than histotype. However, this landscape may change in the era of personalized therapy, given that most subtypes (with the exception of high-grade serous carcinoma) are relatively resistant to chemotherapy. It is now well-accepted that high-grade and low-grade serous carcinomas represent distinct entities rather than a spectrum of the same tumor type. While they are similar in that patients present with advanced-stage disease, their histologic and molecular features are entirely different. High-grade serous carcinoma is associated with TP53 mutations, whereas low-grade serous carcinomas are associated with BRAF and KRAS mutations. Endometrioid and clear cell carcinomas typically present as early-stage disease and are frequently associated with endometriosis. Mucinous carcinomas typically present as large unilateral masses and often show areas of mucinous cystadenoma and mucinous borderline tumor. It must be emphasized that primary mucinous carcinomas are uncommon tumors, and metastasis from other sites such as the appendix, colon, stomach, and pancreaticobiliary tract must always be considered in the differential diagnosis. Lastly, transitional cell tumors of the ovary, specifically malignant Brenner tumors, are quite uncommon. High-grade serous carcinoma often has a transitional cell pattern, and adequate sampling in most cases shows more typical areas of serous carcinoma. Immunohistochemical markers are routinely employed in the diagnosis of epithelial ovarian carcinomas. However, molecular testing of these tumors, unlike in endometrial carcinoma, is not routinely used in clinical practice.

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Year:  2016        PMID: 26892153

Source DB:  PubMed          Journal:  Oncology (Williston Park)        ISSN: 0890-9091            Impact factor:   2.990


  47 in total

1.  Prediction of DNA Repair Inhibitor Response in Short-Term Patient-Derived Ovarian Cancer Organoids.

Authors:  Sarah J Hill; Brennan Decker; Emma A Roberts; Neil S Horowitz; Michael G Muto; Michael J Worley; Colleen M Feltmate; Marisa R Nucci; Elizabeth M Swisher; Huy Nguyen; Chunyu Yang; Ryuji Morizane; Bose S Kochupurakkal; Khanh T Do; Panagiotis A Konstantinopoulos; Joyce F Liu; Joseph V Bonventre; Ursula A Matulonis; Geoffrey I Shapiro; Ross S Berkowitz; Christopher P Crum; Alan D D'Andrea
Journal:  Cancer Discov       Date:  2018-09-13       Impact factor: 39.397

2.  Coexistence of BRAF V600E and TERT Promoter Mutations in Low-grade Serous Carcinoma of Ovary Recurring as Carcinosarcoma in a Lymph Node: Report of a Case.

Authors:  Mahkam Tavallaee; David F Steiner; James L Zehnder; Ann K Folkins; Amer K Karam
Journal:  Int J Gynecol Pathol       Date:  2019-07       Impact factor: 2.762

3.  The CHK1 Inhibitor Prexasertib Exhibits Monotherapy Activity in High-Grade Serous Ovarian Cancer Models and Sensitizes to PARP Inhibition.

Authors:  Kalindi Parmar; Bose S Kochupurakkal; Jean-Bernard Lazaro; Zhigang C Wang; Sangeetha Palakurthi; Paul T Kirschmeier; Chunyu Yang; Larissa A Sambel; Anniina Färkkilä; Elizaveta Reznichenko; Hunter D Reavis; Connor E Dunn; Lee Zou; Khanh T Do; Panagiotis A Konstantinopoulos; Ursula A Matulonis; Joyce F Liu; Alan D D'Andrea; Geoffrey I Shapiro
Journal:  Clin Cancer Res       Date:  2019-08-13       Impact factor: 12.531

4.  Apparent Diffusion Coefficient Histogram Analysis for Assessing Tumor Staging and Detection of Lymph Node Metastasis in Epithelial Ovarian Cancer: Correlation with p53 and Ki-67 Expression.

Authors:  Feng Wang; Yuxiang Wang; Yan Zhou; Congrong Liu; Dong Liang; Lizhi Xie; Zhihang Yao; Jianyu Liu
Journal:  Mol Imaging Biol       Date:  2019-08       Impact factor: 3.488

5.  Extremely long tumor retention, multi-responsive boronate crosslinked micelles with superior therapeutic efficacy for ovarian cancer.

Authors:  Wenwu Xiao; Nell Suby; Kai Xiao; Tzu-Yin Lin; Nasir Al Awwad; Kit S Lam; Yuanpei Li
Journal:  J Control Release       Date:  2017-08-25       Impact factor: 9.776

6.  Potential signaling pathways as therapeutic targets for overcoming chemoresistance in mucinous ovarian cancer.

Authors:  Emiko Niiro; Sachiko Morioka; Kana Iwai; Yuki Yamada; Kenji Ogawa; Naoki Kawahara; Hiroshi Kobayashi
Journal:  Biomed Rep       Date:  2018-01-17

Review 7.  Histone Methyltransferase EZH2: A Therapeutic Target for Ovarian Cancer.

Authors:  Bayley A Jones; Sooryanarayana Varambally; Rebecca C Arend
Journal:  Mol Cancer Ther       Date:  2018-03       Impact factor: 6.261

8.  Identification and validation of core genes for serous ovarian adenocarcinoma via bioinformatics analysis.

Authors:  Ruru Zhu; Jisen Xue; Huijun Chen; Qian Zhang
Journal:  Oncol Lett       Date:  2020-08-21       Impact factor: 2.967

9.  Molecular genetic heterogeneity in undifferentiated endometrial carcinomas.

Authors:  Juan M Rosa-Rosa; Susanna Leskelä; Eva Cristóbal-Lana; Almudena Santón; Ma Ángeles López-García; Gloria Muñoz; Belen Pérez-Mies; Michele Biscuola; Jaime Prat; Oliva Esther; Robert A Soslow; Xavier Matias-Guiu; Jose Palacios
Journal:  Mod Pathol       Date:  2016-08-05       Impact factor: 7.842

10.  BRAFV600E mutations and immunohistochemical expression of VE1 protein in low-grade serous neoplasms of the ovary.

Authors:  Gulisa Turashvili; Rachel N Grisham; Sarah Chiang; Deborah F DeLair; Kay J Park; Robert A Soslow; Rajmohan Murali
Journal:  Histopathology       Date:  2018-06-22       Impact factor: 5.087

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