Literature DB >> 29843906

Endometrial cancer: Molecular markers and management of advanced stage disease.

Rebecca C Arend1, Bayley A Jones2, Alba Martinez3, Paul Goodfellow4.   

Abstract

Endometrial cancer is the most prevalent gynecologic cancer in the United States. Over the last 10 years, death rates from endometrial cancer have been rising about 1.4% per year. Traditionally endometrial cancer treatment has been driven by stage and histology. Recent studies have, however, shown that cancers of the same stage and histology have very distinct molecular and genomic profiles. Translational research is progressing rapidly and endometrial cancer-specific precision medicine is evolving. The first tissue agnostic therapy based on the molecular profile of the tumor was approved by the FDA this year. The approval of immune checkpoint inhibitor, pembrolizumab (anti-PD-1), for all solid tumors with defective DNA mismatch repair, could benefit 20-30% of patients with advanced endometrial cancer. Other genomic changes and molecular markers in endometrial cancer, such as hormone receptor status, could lead to more tailored therapy in the future. Pre-clinical and clinical investigations of targeted therapies suggest efficacy for some agents. Single agent targeted therapies, however, have modest activity. Identifying biomarkers that effectively determine response to targeted therapy remains a challenge. The next generation of clinical trials will focus on novel combinations and how to best utilize the advances that have been made in sequencing technology and bioinformatics. Although there is currently an immense body of data and many options for obtaining genomic characteristics of endometrial cancer, how to interpret and utilize this data is still being explored. This review will summarize the important trials that have led to the treatment options we have for advanced and/or recurrent endometrial cancer and discuss the important studies that have led to a better understanding of the distinctive molecular and genomic profiles within endometrial cancer. We will review the current status of biomarker-driven targeted therapy in endometrial cancer and the rationale behind ongoing clinical trials that are utilizing novel targeted agents.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Advanced disease; Biomarkers; Chemotherapy; Endometrial cancer; Radiation therapy

Mesh:

Substances:

Year:  2018        PMID: 29843906     DOI: 10.1016/j.ygyno.2018.05.015

Source DB:  PubMed          Journal:  Gynecol Oncol        ISSN: 0090-8258            Impact factor:   5.482


  51 in total

1.  CTHRC1 promotes M2-like macrophage recruitment and myometrial invasion in endometrial carcinoma by integrin-Akt signaling pathway.

Authors:  Lu-Ying Li; Ke-Min Yin; Yi-Han Bai; Zhi-Gang Zhang; Wen Di; Shu Zhang
Journal:  Clin Exp Metastasis       Date:  2019-05-22       Impact factor: 5.150

2.  STAT1-induced upregulation of lncRNA LINC01123 predicts poor prognosis and promotes the progression of endometrial cancer through miR-516b/KIF4A.

Authors:  Yuguang Yang; Jin Wu; Hongfeng Zhou; Wenming Liu; Jincai Wang; Qingyuan Zhang
Journal:  Cell Cycle       Date:  2020-05-13       Impact factor: 4.534

3.  Restoration of microRNA-29c in type I endometrioid cancer reduced endometrial cancer cell growth.

Authors:  Michelle Van Sinderen; Meaghan Griffiths; Ellen Menkhorst; Keith Niven; Evdokia Dimitriadis
Journal:  Oncol Lett       Date:  2019-07-09       Impact factor: 2.967

4.  SIX1 Regulates Aberrant Endometrial Epithelial Cell Differentiation and Cancer Latency Following Developmental Estrogenic Chemical Exposure.

Authors:  Alisa A Suen; Wendy N Jefferson; Charles E Wood; Carmen J Williams
Journal:  Mol Cancer Res       Date:  2019-10-09       Impact factor: 5.852

5.  Nuclear receptor 4A1 (NR4A1) antagonists induce ROS-dependent inhibition of mTOR signaling in endometrial cancer.

Authors:  Kumaravel Mohankumar; Xi Li; Subhashree Sridharan; Keshav Karki; Stephen Safe
Journal:  Gynecol Oncol       Date:  2019-04-30       Impact factor: 5.482

6.  BCAT1 promotes proliferation of endometrial cancer cells through reprogrammed BCAA metabolism.

Authors:  Ping Wang; Shouheng Wu; Xiaofeng Zeng; Yaqing Zhang; Ying Zhou; Liuli Su; Wei Lin
Journal:  Int J Clin Exp Pathol       Date:  2018-12-01

Review 7.  Molecular Signatures of Gynecological Cancers: Clinicians Perspective.

Authors:  T S Shylasree; Bansal Richa; Gurram Lavanya; Seema Gulia
Journal:  Indian J Surg Oncol       Date:  2021-02-02

8.  Immunomodulatory Factors in Primary Endometrial Cell Cultures Isolated from Cancer and Noncancerous Human Tissue-Focus on RAGE and IDO1.

Authors:  Joanna Tkaczuk-Włach; Witold Kędzierski; Ilona Jonik; Ilona Sadok; Agata Filip; Marta Kankofer; Wojciech Polkowski; Piotr Ziółkowski; Andrzej Gamian; Magdalena Staniszewska
Journal:  Cells       Date:  2021-04-25       Impact factor: 6.600

9.  B3GNT3 acts as a carcinogenic factor in endometrial cancer via facilitating cell growth, invasion and migration through regulating RhoA/RAC1 pathway-associated markers.

Authors:  Ji-Shui Wang; Fang Ruan; Li-Zhu Guo; Feng-Ge Wang; Fu-Ling Wang; Hong-Min An
Journal:  Genes Genomics       Date:  2021-03-08       Impact factor: 1.839

10.  Enhanced Efficacy of Aurora Kinase Inhibitors in G2/M Checkpoint Deficient TP53 Mutant Uterine Carcinomas Is Linked to the Summation of LKB1-AKT-p53 Interactions.

Authors:  Katherine N Lynch; Joyce F Liu; Nikolas Kesten; Kin-Hoe Chow; Aniket Shetty; Ruiyang He; Mosammat Faria Afreen; Liping Yuan; Ursula A Matulonis; Whitfield B Growdon; Michael G Muto; Neil S Horowitz; Colleen M Feltmate; Michael J Worley; Ross S Berkowitz; Christopher P Crum; Bo R Rueda; Sarah J Hill
Journal:  Cancers (Basel)       Date:  2021-05-03       Impact factor: 6.639

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