References
- Akaev, I., Yeoh, C.C., and Rahimi, S., 2021. Update on endometrial stromal tumours of the uterus. Diagnostics, 11 (3), 429.
- Anglesio, M.S., et al., 2017. Cancer-associated mutations in endometriosis without cancer. New England Journal of Medicine, 376 (19), 1835–1848.
- Arnold, J., et al., 2013. Neuroimmunomodulatory alterations in non-lesional peritoneum close to peritoneal endometriosis. Neuroimmunomodulation, 20 (1), 9–18.
- Bailey, M.L., et al., 2014. Glioblastoma cells containing mutations in the cohesin component STAG2 are sensitive to PARP inhibition. Molecular Cancer Therapeutics, 13 (3), 724–732.
- Barcena de Arellano, M.L., et al., 2013. Evidence of neurotrophic events due to peritoneal endometriotic lesions. Cytokine, 62 (2), 253–261.
- Barcena de Arellano, M.L., et al., 2012. Eutopic endometrium from women with endometriosis does not exhibit neurotrophic properties. Journal of Neuroimmunology, 249 (1–2), 49–55.
- Basak, S. and Saha, A., 2009. Adenomyosis: still largely under-diagnosed. Journal of Obstetrics and Gynaecology, 29 (6), 533–535.
- Bergeron, C., Amant, F., and Ferenczy, A., 2006. Pathology and physiopathology of adenomyosis. Best Practice & Research. Clinical Obstetrics & Gynaecology, 20 (4), 511–521.
- Bhagwate, A.V., et al., 2019. Bioinformatics and DNA-extraction strategies to reliably detect genetic variants from FFPE breast tissue samples. BMC Genomics, 20 (1), 689.
- Bradley, L.D., Falcone, T., and Magen, A.B., 2000. Radiographic imaging techniques for the diagnosis of abnormal uterine bleeding. Obstetrics and Gynecology Clinics of North America, 27 (2), 245–276.
- De Koninck, M. and Losada, A., 2016. Cohesin mutations in cancer. Cold Spring Harbor Perspectives in Medicine, 6 (12), a026476.
- Ferenczy, A., 1998. Pathophysiology of adenomyosis. Human Reproduction Update, 4 (4), 312–322.
- Guan, B., et al., 2012. Functional analysis of in-frame indel ARID1A mutations reveals new regulatory mechanisms of its tumor suppressor functions. Neoplasia, 14 (10), 986–993.
- Hao, B., et al., 2007. Structure of a Fbw7–Skp1–cyclin E complex: multisite-phosphorylated substrate recognition by SCF ubiquitin ligases. Molecular Cell, 26 (1), 131–143.
- Inoue, S., et al., 2019. Uterine adenomyosis is an oligoclonal disorder associated with KRAS mutations. Nature Communications, 10 (1), 5785.
- Krishnan, T., et al., 2022. Targeting mutated KRAS genes to treat solid tumours. Molecular Diagnosis & Therapy, 26 (1), 39–49.
- Lagana, A.S., et al., 2020. Evaluation of M1 and M2 macrophages in ovarian endometriomas from women affected by endometriosis at different stages of the disease. Gynecological Endocrinology, 36 (5), 441–444.
- Lagana, A.S., et al., 2018. Stem cell trafficking during endometriosis: may epigenetics play a pivotal role? Reproductive Sciences, 25 (7), 978–979.
- Levgur, M., Abadi, M.A., and Tucker, A., 2000. Adenomyosis: symptoms, histology, and pregnancy terminations. Obstetrics and Gynecology, 95 (5), 688–691.
- Li, X., et al., 2014. Whole-exome sequencing of endometriosis identifies frequent alterations in genes involved in cell adhesion and chromatin-remodeling complexes. Human Molecular Genetics, 23 (22), 6008–6021.
- Li, Y.W., et al., 2018. Clinical manifestations of adenomyosis patients with or without coexisting endometriosis. Chinese Medical Journal, 131 (20), 2495–2498.
- Reisman, D., Glaros, S., and Thompson, E.A., 2009. The SWI/SNF complex and cancer. Oncogene, 28 (14), 1653–1668.
- Richards, S., et al., 2015. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genetics in Medicine, 17 (5), 405–424.
- Russo, M., et al., 2020. Mutational profile of endometrial hyperplasia and risk of progression to endometrioid adenocarcinoma. Cancer, 126 (12), 2775–2783.
- Solomon, D.A., et al., 2011. Mutational inactivation of STAG2 causes aneuploidy in human cancer. Science, 333 (6045), 1039–1043.
- Suda, K., et al., 2018. Clonal expansion and diversification of cancer-associated mutations in endometriosis and normal endometrium. Cell Reports, 24 (7), 1777–1789.
- Sunkara, S.K. and Khan, K.S., 2012. Adenomyosis and female fertility: a critical review of the evidence. Journal of Obstetrics and Gynaecology, 32 (2), 113–116.
- Tan, M.C., et al., 2015. GNAS and KRAS mutations define separate progression pathways in intraductal papillary mucinous neoplasm-associated carcinoma. Journal of the American College of Surgeons, 220 (5), 845–854.e1.
- Vavilis, D., et al., 1997. Adenomyosis at hysterectomy: prevalence and relationship to operative findings and reproductive and menstrual factors. Clinical and Experimental Obstetrics & Gynecology, 24 (1), 36–38.
- Wang, P.P., et al., 2016. BAM-matcher: a tool for rapid NGS sample matching. Bioinformatics, 32 (17), 2699–2701.
- Xu, C., et al., 2017. Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller. BMC Genomics, 18 (1), 5.
- Yeh, C.H., Bellon, M., and Nicot, C., 2018. FBXW7: a critical tumor suppressor of human cancers. Molecular Cancer, 17 (1), 115.
- Yetimalar, M.H., Kilic, D., and Bezircioglu, I. 2022. The impact of uterine adenomyosis on the histopathological risk factors and survival in patients with endometrial adenocarcinoma. Journal of Obstetrics and Gynaecology, 42, 1–7.