Weiss SW, Tavassoli FA. Multicystic mesothelioma. An analysis of pathologic findings and biologic behavior in 37 cases. Am J Surg Pathol. 1988;12:737–46.
Google Scholar
Nizri E, Baratti D, Guaglio M, Sinukumar S, Cabras A, Kusamura S, et al. Multicystic mesothelioma: operative and long-term outcomes with cytoreductive surgery and hyperthermic intra peritoneal chemotherapy. Eur J Surg Oncol. 2018;44:1100–4.
Google Scholar
Sawh RN, Malpica A, Deavers MT, Liu J, Silva EG. Benign cystic mesothelioma of the peritoneum: a clinicopathologic study of 17 cases and immunohistochemical analysis of estrogen and progesterone receptor status. Hum Pathol. 2003;34:369–74.
Google Scholar
Chua TC, Yan TD, Deraco M, Glehen O, Moran BJ, Sugarbaker PH. Peritoneal Surface Oncology G. Multi-institutional experience of diffuse intra-abdominal multicystic peritoneal mesothelioma. Br J Surg. 2011;98:60–4.
Google Scholar
Sethna K, Mohamed F, Marchettini P, Elias D, Sugarbaker PH. Peritoneal cystic mesothelioma: a case series. Tumori. 2003;89:31–5.
Google Scholar
Carr NJ. Low grade mesothelial tumors of the peritoneum: multicystic mesothelioma, well-differentiated papillary mesothelioma, and adenomatoid tumor. Ajsp-Rev Rep. 2019;24:111–6.
Google Scholar
Ball NJ, Urbanski SJ, Green FH, Kieser T. Pleural multicystic mesothelial proliferation. The so-called multicystic mesothelioma. Am J Surg Pathol. 1990;14:375–8.
Google Scholar
Katsube Y, Mukai K, Silverberg SG. Cystic mesothelioma of the peritoneum: a report of five cases and review of the literature. Cancer. 1982;50:1615–22.
Google Scholar
Sienkowski IK, Russell AJ, Dilly SA, Djazaeri B. Peritoneal cystic mesothelioma: an electron microscopic and immunohistochemical study of two male patients. J Clin Pathol. 1986;39:440–5.
Google Scholar
Zahid A, Clarke L, Carr N, Chandrakumaran K, Tzivanakis A, Dayal S, et al. Outcomes of multicystic peritoneal mesothelioma treatment with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy. BJS Open. 2021;5:zraa001.
Chen X, Sheng W, Wang J. Well-differentiated papillary mesothelioma: a clinicopathological and immunohistochemical study of 18 cases with additional observation. Histopathology. 2013;62:805–13.
Google Scholar
Chan JK, Fong MH. Composite multicystic mesothelioma and adenomatoid tumour of the uterus: different morphological manifestations of the same process?. Histopathology. 1996;29:375–7.
Google Scholar
Panagopoulos I, Gorunova L, Davidson B, Heim S. Novel TNS3-MAP3K3 and ZFPM2-ELF5 fusion genes identified by RNA sequencing in multicystic mesothelioma with t(7;17)(p12;q23) and t(8;11)(q23;p13). Cancer Lett. 2015;357:502–9.
Google Scholar
Engohan-Aloghe C, Anaf V, Noel JC. Lymph node involvement in multicystic peritoneal mesothelioma. Int J Gynecol Pathol. 2009;28:594–7.
Google Scholar
Hiltbrunner S, Fleischmann Z, Sokol ES, Zoche M, Felley-Bosco E, Curioni-Fontecedro A. Genomic landscape of pleural and peritoneal mesothelioma tumours. Br J Cancer. 2022;127:1997–2005.
Google Scholar
Husain AN, Colby TV, Ordonez NG, Allen TC, Attanoos RL, Beasley MB, et al. Guidelines for Pathologic Diagnosis of Malignant Mesothelioma 2017 Update of the Consensus Statement From the International Mesothelioma Interest Group. Arch Pathol Lab Med. 2018;142:89–108.
Google Scholar
Gibson J, Pengelly RJ, Mirandari A, Boukas K, Stanford S, Cecil TD, et al. Targeted genetic sequencing analysis of 223 cases of pseudomyxoma peritonei treated by cytoreductive surgery and hyperthermic intraperitoneal chemotherapy shows survival related to GNAS and KRAS Status. Cancer Med. 2024;13:e70340.
Google Scholar
Pengelly RJ, Gibson J, Andreoletti G, Collins A, Mattocks CJ, Ennis S. A SNP profiling panel for sample tracking in whole-exome sequencing studies. Genome Med. 2013;5:89.
Google Scholar
Barnell EK, Ronning P, Campbell KM, Krysiak K, Ainscough BJ, Sheta LM, et al. Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samples. Genet Med. 2019;21:972–81.
Google Scholar
Elizarraras JM, Liao Y, Shi Z, Zhu Q, Pico AR, Zhang B. WebGestalt 2024: faster gene set analysis and new support for metabolomics and multi-omics. Nucleic Acids Res. 2024;52:W415–W21.
Google Scholar
Abraham MJ, Murtola T, Schulz R, Páll S, Smith JC, Hess B, et al. GROMACS: High performance molecular simulations through multi-level parallelism from laptops to supercomputers. SoftwareX. 2015;1-2:19–25.
Google Scholar
Huang J, Rauscher S, Nawrocki G, Ran T, Feig M, de Groot BL, et al. CHARMM36m: an improved force field for folded and intrinsically disordered proteins. Nat Methods. 2017;14:71–3.
Google Scholar
Shi Z, Gao H, Bai XC, Yu H. Cryo-EM structure of the human cohesin-NIPBL-DNA complex. Science. 2020;368:1454–9.
Google Scholar
Marcos-Alcalde I, Mendieta-Moreno JI, Puisac B, Gil-Rodriguez MC, Hernandez-Marcos M, Soler-Polo D, et al. Two-step ATP-driven opening of cohesin head. Sci Rep. 2017;7:3266.
Google Scholar
Hung YP, Dong F, Torre M, Crum CP, Bueno R, Chirieac LR. Molecular characterization of diffuse malignant peritoneal mesothelioma. Mod Pathol. 2020;33:2269–79.
Google Scholar
Offin M, Yang SR, Egger J, Jayakumaran G, Spencer RS, Lopardo J, et al. Molecular Characterization of Peritoneal Mesotheliomas. J Thorac Oncol. 2022;17:455–60.
Google Scholar
Eckardt JN, Stasik S, Rollig C, Sauer T, Scholl S, Hochhaus A, et al. Alterations of cohesin complex genes in acute myeloid leukemia: differential co-mutations, clinical presentation and impact on outcome. Blood Cancer J. 2023;13:18.
Google Scholar
Guo G, Sun X, Chen C, Wu S, Huang P, Li Z, et al. Whole-genome and whole-exome sequencing of bladder cancer identifies frequent alterations in genes involved in sister chromatid cohesion and segregation. Nat Genet. 2013;45:1459–63.
Google Scholar
Barber TD, McManus K, Yuen KW, Reis M, Parmigiani G, Shen D, et al. Chromatid cohesion defects may underlie chromosome instability in human colorectal cancers. Proc Natl Acad Sci USA. 2008;105:3443–8.
Google Scholar
Ghiselli G, Iozzo RV. Overexpression of bamacan/SMC3 causes transformation. J Biol Chem. 2000;275:20235–8.
Google Scholar
GTExPortal. GTEx Portal [Available from: https://www.gtexportal.org/home/.
Deardorff MA, Kaur M, Yaeger D, Rampuria A, Korolev S, Pie J, et al. Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation. Am J Hum Genet. 2007;80:485–94.
Google Scholar
Heath AP, Ferretti V, Agrawal S, An M, Angelakos JC, Arya R, et al. The NCI Genomic Data Commons. Nat Genet. 2021;53:257–62.
Google Scholar
Ladurner R, Bhaskara V, Huis in ‘t Veld PJ, Davidson IF, Kreidl E, Petzold G, et al. Cohesin’s ATPase activity couples cohesin loading onto DNA with Smc3 acetylation. Curr Biol. 2014;24:2228–37.
Google Scholar
Orelle C, Dalmas O, Gros P, Di Pietro A, Jault JM. The conserved glutamate residue adjacent to the Walker-B motif is the catalytic base for ATP hydrolysis in the ATP-binding cassette transporter BmrA. J Biol Chem. 2003;278:47002–8.
Google Scholar
Smith PC, Karpowich N, Millen L, Moody JE, Rosen J, Thomas PJ, et al. ATP binding to the motor domain from an ABC transporter drives formation of a nucleotide sandwich dimer. Mol Cell. 2002;10:139–49.
Google Scholar
Sobti M, Ueno H, Noji H, Stewart AG. The six steps of the complete F(1)-ATPase rotary catalytic cycle. Nat Commun. 2021;12:4690.
Google Scholar
Vitoria Gomes M, Landwerlin P, Diebold-Durand ML, Shaik TB, Durand A, Troesch E, et al. The cohesin ATPase cycle is mediated by specific conformational dynamics and interface plasticity of SMC1A and SMC3 ATPase domains. Cell Rep. 2024;43:114656.
Google Scholar
Antony J, Chin CV, Horsfield JA. Cohesin mutations in cancer: emerging therapeutic targets. Int J Mol Sci. 2021;22:6788.
Rittenhouse NL, Carico ZM, Liu YF, Stefan HC, Arruda NL, Zhou J, et al. Functional impact of cancer-associated cohesin variants on gene expression and cellular identity. Genetics. 2021;217:iyab025.
