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      Hormone receptor expression of colorectal cancer diagnosed during the peri-partum period

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          Abstract

          Background

          Colorectal carcinoma (CRC) during the peri-partum period is challenging to diagnose due to the overlapping symptoms of CRC and pregnancy. This is the first case series to investigate clinicopathologic, hormonal and molecular features of CRC diagnosed during the peri-partum period. We hypothesized that advanced presentations of CRC could possibly be mitigated by pregnancy-related hormonal factors.

          Methods

          We conducted a retrospective review of five women diagnosed with CRC during the peri-partum period and studied the clinical and molecular features of their cancer.

          Results

          All patients presented with stage IV CRC at diagnosis; three had primary tumors in the rectum and two had primary tumors in the sigmoid colon. The liver was the most common metastatic site (three of five women). Immunohistochemistry stains were negative for estrogen receptors alpha (ERα) and beta (ERβ), and one tumor demonstrated low-level positivity for PR (1%). Formalin-fixed and paraffin-embedded (FFPE) biopsies from each case were tested with next-generation sequencing and found that all tumors were mismatch repair (MMR) proficient, and three harbored a KRAS mutation. Germline testing showed no predisposition to CRC; however, several somatic variants of undetermined significance (VUS) were identified.

          Discussion

          CRC in the peri-partum period poses significant risk factors for presentations with advanced disease due to diagnostic challenges. While our study provides no evidence that pathogenesis of CRC during pregnancy is driven by elevated estrogen and/or progesterone levels during pregnancy, additional putative etiologic factors, including placental growth factors, the immunosuppressive state of pregnancy and other physiologic processes during pregnancy, warrant future study.

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          Most cited references38

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          Screening for Colorectal Cancer: US Preventive Services Task Force Recommendation Statement.

          Colorectal cancer is the second leading cause of cancer death in the United States. In 2016, an estimated 134,000 persons will be diagnosed with the disease, and about 49,000 will die from it. Colorectal cancer is most frequently diagnosed among adults aged 65 to 74 years; the median age at death from colorectal cancer is 68 years.
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            Colorectal Cancer Incidence Patterns in the United States, 1974-2013.

            Colorectal cancer (CRC) incidence in the United States is declining rapidly overall but, curiously, is increasing among young adults. Age-specific and birth cohort patterns can provide etiologic clues, but have not been recently examined.
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              Clinical Sequencing Defines the Genomic Landscape of Metastatic Colorectal Cancer

              Metastatic colorectal cancers (mCRCs) are clinically heterogeneous, but the genomic basis of this variability remains poorly understood. We performed prospective targeted sequencing of 1134 CRCs. We identified splice alterations in intronic regions of APC and large in-frame deletions in CTNNB1 , increasing oncogenic WNT pathway alterations to 96% of CRCs. Right-sided primary site in microsatellite stable mCRC was associated with shorter survival, older age at diagnosis, increased mutations, and enrichment of oncogenic alterations in KRAS , BRAF , PIK3CA , AKT1 , RNF43 , and SMAD4 compared to left-sided primaries. Left-sided tumors frequently had no identifiable genetic alteration in mitogenic signaling, but exhibited higher mitogenic ligand expression. Our results suggest different pathways to tumorigenesis in right- and left-sided microsatellite stable CRC that may underlie clinical differences.

                Author and article information

                Journal
                Endocr Connect
                Endocr Connect
                EC
                Endocrine Connections
                Bioscientifica Ltd (Bristol )
                2049-3614
                August 2019
                10 July 2019
                : 8
                : 8
                : 1149-1158
                Affiliations
                [1 ]Helen Diller Family Comprehensive Cancer Center , University of California, San Francisco, California, USA
                [2 ]Division of Hematology and Oncology , Department of Medicine, University of California, San Francisco, California, USA
                [3 ]Department of Obstetrics , Gynecology and Reproductive Sciences, University of California, San Francisco, California, USA
                [4 ]Department of Radiology and Biomedical Imaging , University of California, San Francisco, California, USA
                [5 ]Department of Pathology , University of California, San Francisco, California, USA
                Author notes
                Correspondence should be addressed to K Van Loon: katherine.vanloon@ 123456ucsf.edu
                Article
                EC-19-0063
                10.1530/EC-19-0063
                6686950
                31370007
                d26fdffb-2162-4100-8367-9385d9c4468f
                © 2019 The authors

                This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

                History
                : 22 May 2019
                : 10 July 2019
                Categories
                Research

                colorectal cancer,pregnancy,estrogen,progesterone,molecular features

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