دورية أكاديمية

HNF4A and GATA6 Loss Reveals Therapeutically Actionable Subtypes in Pancreatic Cancer

التفاصيل البيبلوغرافية
العنوان: HNF4A and GATA6 Loss Reveals Therapeutically Actionable Subtypes in Pancreatic Cancer
المؤلفون: Brunton H., Caligiuri G., Cunningham R., Upstill-Goddard R., Bailey, U. -M., Garner I. M., Nourse C., Dreyer S., Jones M., Moran-Jones K., Wright D. W., Paulus-Hock V., Nixon C., Thomson G., Jamieson N. B., McGregor G. A., Evers L., McKay C. J., Gulati A., Brough R., Bajrami I., Pettitt S. J., Dziubinski M. L., Barry S. T., Grützmann R., Brown R., Curry E., Allison S., Biankin A. V., Chang D. K., Cooke S. L., Grimwood P., Kelly S., Marshall J., McDade B., McElroy D., Ramsay D., Rebus S., Hair J., Westwood P., Williams N., Duthie F., Johns A. L., Mawson A., Scarlett C. J., Brancato, M. -A. L., Rowe S. J., Simpson S. H., Martyn-Smith M., Thomas M. T., Chantrill L. A., Chin V. T., Chou A., Cowley M. J., Humphris J. L., Mead R. S., Nagrial A. M., Pajic M., Pettit J., Pinese M., Rooman I., Wu J., Tao J., DiPietro R., Watson C., Steinmann A., Lee H. C., Wong R., Pinho A. V., Giry-Laterriere M., Daly R. J., Musgrove E. A., Sutherland R. L., Grimmond S. M., Waddell N., Kassahn K. S., Miller D. K., Wilson P. J., Patch, A. -M., Song S., Harliwong I., Idrisoglu S., Nourbakhsh E., Manning S., Wani S., Gongora M., Anderson M., Holmes O., Leonard C., Taylor D., Wood S., Xu C., Nones K., Fink J. L., Christ A., Bruxner T., Cloonan N., Newell F., Pearson J. V., Quinn M., Nagaraj S., Kazakoff S., Krisnan K., Quek K., Wood D., Samra J. S., Gill A. J., Pavlakis N., Guminski A., Toon C., Asghari R., Merrett N. D., Pavey D., Das A., Cosman P. H., Ismail K., O'Connnor C., Lam V. W., McLeod D., Pleass H. C., Richardson A., James V., Kench J. G., Cooper C. L., Joseph D., Sandroussi C., Crawford M., Gallagher J., Texler M., Forest C., Laycock A., Epari K. P., Ballal M., Fletcher D. R., Mukhedkar S., Spry N. A., DeBoer B., Chai M., Zeps N., Beilin M., Feeney K., Nguyen N. Q., Ruszkiewicz A. R., Worthley C., Tan C. P., Debrencini T., Chen J., Brooke-Smith M. E., Papangelis V., Tang H., Barbour A. P., Clouston A. D., Martin P., O'Rourke T. J., Chiang A., Fawcett J. W., Slater K., Yeung S., Hatzifotis M., Hodgkinson P., Christophi C., Nikfarjam M., Mountain A., Eshleman J. R., Hruban R. H., Maitra A., Iacobuzio-Donahue C. A., Schulick R. D., Wolfgang C. L., Morgan R. A., Hodgin M., Scarpa A., Lawlor R. T., Beghelli S., Corbo V., Scardoni M., Bassi C., Tempero M. A., Graham J. S., Petersen G. M., Shanks E., Ashworth A., Crawford H. C., Simeone D. M., Froeling F. E. M., Lord C. J., Mukhopadhyay D., Pilarsky C., Grimmond S. E., Morton J. P., Sansom O. J., Bailey P. J.
المساهمون: Brunton, H., Caligiuri, G., Cunningham, R., Upstill-Goddard, R., Bailey, U., -M., Garner, I. M., Nourse, C., Dreyer, S., Jones, M., Moran-Jones, K., Wright, D. W., Paulus-Hock, V., Nixon, C., Thomson, G., Jamieson, N. B., Mcgregor, G. A., Evers, L., Mckay, C. J., Gulati, A., Brough, R., Bajrami, I., Pettitt, S. J., Dziubinski, M. L., Barry, S. T., Grützmann, R., Brown, R., Curry, E., Allison, S., Biankin, A. V., Chang, D. K., Cooke, S. L., Grimwood, P., Kelly, S., Marshall, J., Mcdade, B., Mcelroy, D., Ramsay, D., Rebus, S., Hair, J., Westwood, P., Williams, N., Duthie, F., Johns, A. L., Mawson, A., Scarlett, C. J., Brancato, M. -A., L., Rowe, S. J., Simpson, S. H., Martyn-Smith, M., Thomas, M. T., Chantrill, L. A., Chin, V. T., Chou, A., Cowley, M. J., Humphris, J. L., Mead, R. S., Nagrial, A. M., Pajic, M., Pettit, J., Pinese, M., Rooman, I., Wu, J., Tao, J., Dipietro, R., Watson, C., Steinmann, A., Lee, H. C., Wong, R., Pinho, A. V., Giry-Laterriere, M., Daly, R. J., Musgrove, E. A., Sutherland, R. L., Grimmond, S. M., Waddell, N., Kassahn, K. S., Miller, D. K., Wilson, P. J., Patch, A., -M., Song, S., Harliwong, I., Idrisoglu, S., Nourbakhsh, E., Manning, S., Wani, S., Gongora, M., Anderson, M., Holmes, O., Leonard, C., Taylor, D., Wood, S., Xu, C., Nones, K., Fink, J. L., Christ, A., Bruxner, T., Cloonan, N.
سنة النشر: 2020
المجموعة: Università degli Studi di Verona: Catalogo dei Prodotti della Ricerca (IRIS)
مصطلحات موضوعية: GATA6, GSK3B, HNF4A, PDAC subtypes, chromatin landscapes, intronic and distal promoters, metabolic targeting, therapeutic tolerance
الوصف: Pancreatic ductal adenocarcinoma (PDAC) can be divided into transcriptomic subtypes with two broad lineages referred to as classical (pancreatic) and squamous. We find that these two subtypes are driven by distinct metabolic phenotypes. Loss of genes that drive endodermal lineage specification, HNF4A and GATA6, switch metabolic profiles from classical (pancreatic) to predominantly squamous, with glycogen synthase kinase 3 beta (GSK3 beta) a key regulator of glycolysis. Pharmacological inhibition of GSK3 beta results in selective sensitivity in the squamous subtype; however, a subset of these squamous patient-derived cell lines (PDCLs) acquires rapid drug tolerance. Using chromatin accessibility maps, we demonstrate that the squamous subtype can be further classified using chromatin accessibility to predict responsiveness and tolerance to GSK3 beta inhibitors. Our findings demonstrate that distinct patterns of chromatin accessibility can be used to identify patient subgroups that are indistinguishable by gene expression profiles, highlighting the utility of chromatin-based biomarkers for patient selection in the treatment of PDAC.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32402285; info:eu-repo/semantics/altIdentifier/wos/WOS:000533147000008; volume:31; issue:6; firstpage:107625; lastpage:107652; numberofpages:28; journal:CELL REPORTS; http://hdl.handle.net/11562/1031969Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85084363031
DOI: 10.1016/j.celrep.2020.107625
الإتاحة: https://doi.org/10.1016/j.celrep.2020.107625Test
http://hdl.handle.net/11562/1031969Test
رقم الانضمام: edsbas.EB7C6B98
قاعدة البيانات: BASE