The DOI matches its Crossref record; 70 of the 70 references it cites were found in a registry or an index.
Mutant GNAS drives pancreatic tumourigenesis by inducing PKA-mediated SIK suppression and reprogramming lipid metabolism
Open accessAbstract
G protein α s (GNAS) mediates receptor-stimulated cAMP signalling, which integrates diverse environmental cues with intracellular responses. GNAS is mutationally activated in multiple tumour types, although its oncogenic mechanisms remain elusive. We explored this question in pancreatic tumourigenesis where concurrent GNAS and KRAS mutations characterize pancreatic ductal adenocarcinomas (PDAs) arising from intraductal papillary mucinous neoplasms (IPMNs). By developing genetically engineered mouse models, we show that Gnas R201C cooperates with Kras G12D to promote initiation of IPMN, which progress to invasive PDA following Tp53 loss. Mutant Gnas remains critical for tumour maintenance in vivo. This is driven by protein-kinase-A-mediated suppression of salt-inducible kinases (Sik1-3), associated with induction of lipid remodelling and fatty acid oxidation. Comparison of Kras-mutant pancreatic cancer cells with and without Gnas mutations reveals striking differences in the functions of this network. Thus, we uncover Gnas-driven oncogenic mechanisms, identify Siks as potent tumour suppressors, and demonstrate unanticipated metabolic heterogeneity among Kras-mutant pancreatic neoplasms.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“More recent IPMN models have been generated that genocopy recurrent driver alterations observed in cognate human lesions (i.e. Kras, Gnas, Rnf43) (Fig 1)34–36, and these models demonstrate the comparable stepwise progression observed in patient derived IPMNs.”
From Pancreatic cancer: Advances and challenges (2023) · cites this paper as [35]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Subramanian, A., Tamayo, P., Mootha, V. K., Mukherjee, S., Ebert, B. L., Gillette, M. A., Paulovich, A., Pomeroy, S. L., Golub, T. R., Lander, E. S., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506580102 · Cited by 53,625
Improved vectors and genome-wide libraries for CRISPR screening
Sanjana, N. E., Shalem, O., & Zhang, F. (2014) · Nature Methods · doi:10.1038/nmeth.3047 · Cited by 5,239
Genomic analyses identify molecular subtypes of pancreatic cancer
Bailey, P., Chang, D. K., Nones, K., Johns, A. L., Patch, A.-M., Gingras, M.-C., Miller, D. K., Christ, A. N., Bruxner, T. J. C., Quinn, M. C., et al. (2016) · Nature · doi:10.1038/nature16965 · Cited by 3,621
Zehir, A., Benayed, R., Shah, R. H., Syed, A., Middha, S., Kim, H. R., Srinivasan, P., Gao, J., Chakravarty, D., Devlin, S. M., et al. (2017) · Nature Medicine · doi:10.1038/nm.4333 · Cited by 3,380
Fatty acid synthase and the lipogenic phenotype in cancer pathogenesis
Menendez, J. A., & Lupu, R. (2007) · Nature Reviews Cancer · doi:10.1038/nrc2222 · Cited by 2,941
Trends in GPCR drug discovery: new agents, targets and indications
Hauser, A. S., Attwood, M. M., Rask‐Andersen, M., Schiöth, H. B., & Gloriam, D. E. I. (2017) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2017.178 · Cited by 2,714
Cellular Fatty Acid Metabolism and Cancer
Currie, E., Schulze, A., Zechner, R., Walther, T. C., & Farese, R. V. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.05.017 · Cited by 2,123
Oncogenic Kras maintains pancreatic tumors through regulation of anabolic glucose metabolism
Ying, H., Kimmelman, A. C., Lyssiotis, C. A., Hua, S., Chu, G. C., Fletcher-Sananikone, E., Locasale, J. W., Son, J., Zhang, H., Coloff, J. L., et al. (2012) · Cell · doi:10.1016/j.cell.2012.01.058 · Cited by 2,043
Integrated genomic characterization of pancreatic ductal adenocarcinoma
Raphael, B. J., Hruban, R. H., Aguirre, A. J., Moffitt, R. A., Yeh, J. J., Stewart, C., Robertson, A. G., Cherniack, A. D., Gupta, M., Getz, G., et al. (2017) · Cancer Cell · doi:10.1016/j.ccell.2017.07.007 · Cited by 2,019
Self-citationThe LKB1-AMPK pathway: metabolism and growth control in tumour suppression
Shackelford, D. B., & Shaw, R. J. (2009) · Nature Reviews Cancer · doi:10.1038/nrc2676 · Cited by 1,943
Cited by
Sorted by citations
Items 101–192 of 192
Genetic Signature of Human Pancreatic Cancer and Personalized Targeting
Reshkin, S. J., Cardone, R. A., & Koltai, T. (2024) · Cells · doi:10.3390/cells13070602 · Cited by 14
Hu, D., Du, J., Xing, Y., Cheng, Y., He, R., Liang, X., Li, H., & Yang, Y. (2023) · Journal of obstetrics and gynaecology research · doi:10.1111/jog.15714 · Cited by 13
Multi-omic markers of intraductal papillary mucinous neoplasms progression into pancreatic cancer
Corradi, C., Gentiluomo, M., Adsay, V. N., Sáinz, J., Camisa, P. R., Włodarczyk, B., Crippa, S., Tavano, F., Capurso, G., & Campa, D. (2024) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2024.12.005 · Cited by 12
Maeda, C., Ono, Y., Hayashi, A., Takahashi, K., Taniue, K., Kakisaka, R., Mori, M., Ishii, T. M., Sato, H., Okada, T., et al. (2023) · Journal of Molecular Diagnostics · doi:10.1016/j.jmoldx.2023.02.007 · Cited by 12
Self-citationInsights into the tumor-stromal-immune cell metabolism cross talk in ovarian cancer
Tang, P. W., Frisbie, L. G., Hempel, N., & Coffman, L. G. (2023) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00588.2022 · Cited by 10
Bahado-Singh, R. O., Türkoğlu, O., Aydas, B., & Vishweswaraiah, S. (2023) · Cancer Medicine · doi:10.1002/cam4.6604 · Cited by 11
Exploring the Common Mutational Landscape in Cutaneous Melanoma and Pancreatic Cancer
Broseghini, E., Venturi, F., Veronesi, G., Scotti, B., Migliori, M., Marini, D., Ricci, C., Casadei, R., Ferracin, M., & Dika, E. (2024) · Pigment Cell & Melanoma Research · doi:10.1111/pcmr.13210 · Cited by 10
Metabolic plasticity in pancreatic ductal adenocarcinoma progression and response to treatment
Ma, J., Bhardwaj, V., Lobie, P. E., & Pandey, V. (2026) · Molecular Cancer · doi:10.1186/s12943-026-02620-x · Cited by 10
Desai, R., Huang, L., González, R. S., & Muthuswamy, S. K. (2024) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-23-0199 · Cited by 9
Cellular collusion: cracking the code of immunosuppression and chemo resistance in PDAC
Musiu, C., Lupo, F., Agostini, A., Lionetto, G., Bevere, M., Paiella, S., Carbone, C., Corbo, V., Ugel, S., & Sanctis, F. D. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1341079 · Cited by 9
Combined Systemic Drug Treatment with Proton Therapy: Investigations on Patient-Derived Organoids
Naumann, M., Czempiel, T., Lößner, A. J., Pape, K., Beyreuther, E., Löck, S., Drukewitz, S., Hennig, A., von Neubeck, C., Klink, B., et al. (2022) · Cancers · doi:10.3390/cancers14153781 · Cited by 9
Clinical and Molecular Attributes and Evaluation of Pancreatic Cystic Neoplasm
Raut, P., Nimmakayala, R. K., Batra, S. K., & Ponnusamy, M. P. (2022) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2022.188851 · Cited by 10
Primary Resistance to RET Inhibition in a RET Fusion-Positive Pancreatic Neuroendocrine Carcinoma
McKinley, B., Coston, T. W., & Starr, J. S. (2024) · The Oncologist · doi:10.1093/oncolo/oyae034 · Cited by 8
Cholesterol Activates Cyclic AMP Signaling in Metaplastic Acinar Cells
Grisan, F., Spacci, M., Paoli, C., Costamagna, A., Fantuz, M., Martini, M., Lefkimmiatis, K., & Carrer, A. (2021) · Metabolites · doi:10.3390/metabo11030141 · Cited by 8
Active Gα i/o Mutants Accelerate Breast Tumor Metastasis via the c-Src Pathway
Lyu, C., Bhimani, A. K., Draus, W. T., Weigel, R. J., & Chen, S. (2023) · Molecular and Cellular Biology · doi:10.1080/10985549.2023.2285833 · Cited by 8
Road map for fibrolamellar carcinoma: progress and goals of a diversified approach
Kastenhuber, E. R., Craig, J., Ramsey, J. E., Sullivan, K. M., Sage, J., de Oliveira, S., Riehle, K. J., Scott, J. D., Gordan, J. D., Bardeesy, N. M., et al. (2019) · Journal of Hepatocellular Carcinoma · doi:10.2147/jhc.s194764 · Cited by 9
Self-citationAblation of Gsa impairs renal tubule proliferation after injury via CDK2/cyclin E
Liu, L., Deng, Y., Cai, Y., Lu, P., Guo, Y., Zhang, C., Li, Q., Zhang, T., Han, M. H., & Xu, G. (2020) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00367.2019 · Cited by 8
Wang, R., Gao, C., Fan, Z., Qin, Q., & Zhan, H. (2025) · Cancer Letters · doi:10.1016/j.canlet.2025.217965 · Cited by 7
Stress and Obesity Signaling Converge on CREB Phosphorylation to Promote Pancreatic Cancer
Sun, X., Teper, Y., Sinnett‐Smith, J. W., Markarian, M., Hines, O. J., Li, G., Eibl, G., & Rozengurt, E. (2024) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-24-0785 · Cited by 7
Watanabe, K., Nakamura, T., Onodera, S., Saito, A., Shibahara, T., & Azuma, T. (2020) · Tumor Biology · doi:10.1177/1010428320962588 · Cited by 7
Hong, W., Shan, C., Ye, M., Yang, Y., Wang, H., Du, F., Zhang, X., Song, C., & Cai, L. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.737523 · Cited by 7
Salihoğlu, R., Nieves, J., Dandekar, G., Ebert, R., Rudert, M., Dandekar, T., & Bencúrová, E. (2025) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2025.09.028 · Cited by 6
Understanding the Conundrum of Pancreatic Cancer in the Omics Sciences Era
Nicoletti, A., Paratore, M., Vitale, F., Negri, M., Quero, G., Esposto, G., Mignini, I., Alfieri, S., Gasbarrini, A., Zocco, M. A., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25147623 · Cited by 8
Going Rogue: Mechanisms, Regulation, and Roles of Mutationally Activated Gα in Human Cancer
Dwyer, M. B., Aumiller, J. L., & Wedegaertner, P. (2024) · Molecular Pharmacology · doi:10.1124/molpharm.124.000743 · Cited by 5
Elevated SREBP1 accelerates the initiation and growth of pancreatic cancer by targeting SOX9
Zhou, C., Feng, Z., Qian, W., Zhu, Z., Cao, R., Wang, Q., Zhang, W., Liu, R., Wu, S., Hao, J., et al. (2025) · Biology Direct · doi:10.1186/s13062-025-00595-1 · Cited by 6
Contract to kill: GNAS mutation
Raut, P., Mathivanan, P., Batra, S. K., & Ponnusamy, M. P. (2025) · Molecular Cancer · doi:10.1186/s12943-025-02247-4 · Cited by 6
Geng, C., Dong, K., An, J., Liu, Z., Zhao, Q., & Lv, Y. (2025) · Cancer Cell International · doi:10.1186/s12935-025-03822-x · Cited by 6
Sans, M., Chen, Y., Thege, F. I., Dou, R., Min, J., Yip-Schneider, M., Zhang, J., Wu, R., Irajizad, E., Makino, Y., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.14.553002 · Cited by 6
Yang, S., Chen, T., Cui, M., & Hu, Y. N. (2025) · International Journal of Surgery · doi:10.1097/js9.0000000000002814 · Cited by 6
The Hippo signaling pathway modulates pancreatic tissue homeostasis
Wang, X., Du, J., Li, H., Cao, Z., Cheng, Z., & Wang, Z. (2025) · Cell Death Discovery · doi:10.1038/s41420-025-02636-0 · Cited by 6
Osteosarcoma’s genetic landscape painted by genes’ mutations
Urban, W., Krzystańska, D., Piekarz, M., Nazar, J., & Jankowska, A. (2023) · Acta Biochimica Polonica · doi:10.18388/abp.2020_6869 · Cited by 6
He, S., Li, Y., Wang, L., Li, Y., Xu, L., Cai, D., Zhou, J., & Yu, L. (2024) · Neoplasia · doi:10.1016/j.neo.2024.100965 · Cited by 5
Unveiling the Role of Sik1 in Osteoblast Differentiation: Implications for Osteoarthritis
Tian, K., He, X., Lin, X., Chen, X., Su, Y., Lu, Z., Chen, Z., Zhang, L., Li, P., Ma, L., et al. (2024) · Molecular and Cellular Biology · doi:10.1080/10985549.2024.2385633 · Cited by 5
He, M. Y., Tong, K. I., Liu, T., Hawkins, R. W., Shelton, V., Zeng, Y., Bakhtiari, M., Xiao, Y., Zheng, G., Sakhdari, A., et al. (2024) · Leukemia · doi:10.1038/s41375-024-02325-4 · Cited by 5
Chen, Y., Ballarò, R., Sans, M., Thege, F. I., Zuo, M., Dou, R., Min, J., Yip-Schneider, M., Zhang, J., Wu, R., et al. (2025) · Gut · doi:10.1136/gutjnl-2025-335220 · Cited by 6
Ding, L., Roeck, K., Zhang, C., Zidek, B., Rodman, E., Hernandez-Barco, Y. G., Zhang, J.-S., Bamlet, W., Oberg, A., Zhang, L.-Z., et al. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.853003 · Cited by 6
Self-citationZhang, J., Song, Q., & Hu, W. (2024) · Translational Oncology · doi:10.1016/j.tranon.2024.102011 · Cited by 4
Németh, K., Mezei, E., Vörös, J., Borka, K., Pesti, A., Kenessey, I., Kiss, A., & Budai, A. (2025) · The Journal of Pathology Clinical Research · doi:10.1002/2056-4538.70019 · Cited by 4
Tanaka, J., Nakagawa, T., Ono, Y., Kamura, Y., Ishida, T., Kawabata, H., Takahashi, K., Sato, H., Liss, A. S., Mizukami, Y., et al. (2025) · Molecular Oncology · doi:10.1002/1878-0261.70011 · Cited by 4
Self-citationScreening of Therapeutic Targets for Pancreatic Cancer by Bioinformatics Methods
Xiao, X., Wan, Z., Liu, X., Chen, H., Zhao, X., Ding, R., Cao, Y., Zhou, F., Qiu, E., Liang, W., et al. (2023) · Hormone and Metabolic Research · doi:10.1055/a-2007-2715 · Cited by 4
The PDE4DIP-AKAP9 axis promotes lung cancer growth through modulation of PKA signalling
Fu, Y., Huang, S., Pan, R., Chen, X., Liu, T., Zhang, R. X., Zhu, F., Fang, Q., Wu, L., Dai, J., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-07621-y · Cited by 3
YANG, Y., Song, J., Guo, M., Ma, R., Du, M., Xun, Z., Liu, X., Xu, R., Xie, X., Qi, P., et al. (2025) · Advanced Science · doi:10.1002/advs.202511813 · Cited by 3
Lee, M. W., Park, J. M., Cho, I. R., Chung, K. H., Kim, B. S., Choi, J. H., Paik, W. H., Ryu, J. K., Han, K., & Lee, S. H. (2025) · World Journal of Gastroenterology · doi:10.3748/wjg.v31.i40.110932 · Cited by 4
Makino, Y., Oyama, K., Sagara, A., Thege, F. I., & Maitra, A. (2025) · Journal of Gastroenterology · doi:10.1007/s00535-025-02328-7 · Cited by 4
Hu, W., Chen, Z. M., Xue, X. F., Li, X., Yang, G. H., Zhai, Z. Y., Huang, Z. Y., Zhou, P., Bao, C. J., You, L. J., et al. (2024) · Cancer Medicine · doi:10.1002/cam4.70290 · Cited by 3
Intraductal Papillary Mucinous Neoplasm and Pancreatic Cancer: Opportunity Knocks Twice
Hamada, T., Oyama, H., Nakai, Y., Petrov, M. S., & for the TOP-CREATE study group (2025) · The American Journal of Gastroenterology · doi:10.14309/ajg.0000000000003677 · Cited by 3
Yu, Y., Chang, K., Chen, J., Bohlender, R. J., Fowler, J., Zhang, D., Huang, M., Chang, P., Li, Y., Wong, J., et al. (2021) · Human Genetics and Genomics Advances · doi:10.1016/j.xhgg.2021.100078 · Cited by 3
Light-gated integrator for highlighting kinase activity in living cells
Lin, W., Phatarphekar, A., Zhong, Y., Liu, L., Kwon, H., Gerwick, W. H., Wang, Y., Mehta, S., & Zhang, J. (2024) · Nature Communications · doi:10.1038/s41467-024-51270-4 · Cited by 3
Juvenile Granulosa Cell Tumor as the Presenting Feature of McCune-Albright Syndrome
Marks, B. E., Sugrue, R. P., Bourgeois, W., Frazier, A. L., Voss, S. D., Laufer, M. R., Gordon, C. M., & Cohen, L. E. (2021) · Journal of the Endocrine Society · doi:10.1210/jendso/bvab098 · Cited by 3
Yang, S., Hu, Y., Cui, M., Xu, Q., Han, X., Chang, X., Zheng, Q., Xiao, J., Chen, T., Li, P., et al. (2025) · Cancer Letters · doi:10.1016/j.canlet.2025.217730 · Cited by 2
Maeda, C., Yusuke, O. N. O., TAKAHASHI, K., Mori, M., Suzuki, M., Tamamura, N., Sun, Y., Itoh, T., Tanaka, H., Kawabata, H., et al. (2025) · Clinical Chemistry · doi:10.1093/clinchem/hvaf181 · Cited by 2
Self-citationInhibitory probes for spatiotemporal analysis of Gαs protein signaling
Zhao, J., Luebbers, A., Savransky, S., Lin, T.-Y., Cheng, N., Wilcox, A., Janicot, R., Green, E., Sharma, A., Maziarz, M., et al. (2026) · Nature Chemical Biology · doi:10.1038/s41589-025-02138-1 · Cited by 3
Hayes, E. T., Hassan, M., Lakomy, O., Filzen, R., Armouti, M., Foretz, M., Tsumaki, N., Takemori, H., & Stocco, C. O. (2024) · Endocrinology · doi:10.1210/endocr/bqae107 · Cited by 2
Mutated G proteins as drug targets
van der Dussen, K. N., & Jespers, W. (2025) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2025.07.003 · Cited by 2
Nagamine, Y., Tomita, M., Yamakuchi, M., Hozaka, Y., Okumura, T., Oi, H., Fukuda, K., Idichi, T., Yamasaki, Y., Mataki, Y., et al. (2025) · Pancreatology · doi:10.1016/j.pan.2025.09.028 · Cited by 2
Novel modes of MPL activation in triple-negative myeloproliferative neoplasms
Samaraweera, S. E., Geukens, T., Casolari, D. A., Nguyen, T., Sun, C., Bailey, S., Moore, S., Feng, J., SCHREIBER, A. W., Parker, W. T., et al. (2022) · Pathology · doi:10.1016/j.pathol.2022.05.015 · Cited by 2
Pancreatic plasticity: Unlocking exocrine lineage specification
Pitarresi, J. R., & Rustgi, A. K. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.05.006 · Cited by 2
Protein kinase a regulates cyclooxygenase-2 expression through the RNA-binding proteins HuR and TTP
Adame-Garcia, S. R., Hoang, T. S., Vo, P. T. T., Burghi, V., Cervantes‐Villagrana, R. D., Orduña-Castillo, L. B., Ramms, D. J., Trejo, J., & Gutkind, J. S. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.111064 · Cited by 1
Small-molecule activation of the tumor suppressor kinase LKB1 via the pseudokinase STRAD
Song, L., Mitchell, D. C., Liu, J., Leak, L. B., Turnham, R. E., Wang, L., Wang, Z., He, C., Ding, L., Adler, M., et al. (2026) · Cell chemical biology · doi:10.1016/j.chembiol.2026.07.013 · Cited by 3
Gaujoux, S., Parvanescu, A., Fusco, G., Linglart, A., Sauvanet, A., Couvelard, A., Lévy, P., Rebours, V., & Cros, J. F. (2021) · Pancreas · doi:10.1097/mpa.0000000000001732 · Cited by 1
Sawai, H., Kiriyama, Y., Kuzuya, H., Fujii, Y., Ueno, S., Koide, S., Kurimoto, M., Yamao, K., Matsuo, Y., Morimoto, M., et al. (2023) · Journal of Medical Case Reports · doi:10.1186/s13256-023-03798-0 · Cited by 1
KRAS Wild-Type Pancreatic Cancer: Decoding Genomics, Unlocking Therapeutic Potential
Kato, H., Ellis, H., & Bardeesy, N. M. (2023) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-23-2221 · Cited by 1
Self-citationNew Therapeutic Targets in RAS Wild-type Pancreatic Cancer
Diab, M. (2024) · Current Treatment Options in Oncology · doi:10.1007/s11864-024-01242-z · Cited by 1
Unraveling the link between GNAS R201 mutation and colorectal cancer
Behmanesh, M. A., Rafiee, P., Eidikhosh, F., & Moridnia, A. (2025) · Scientific Reports · doi:10.1038/s41598-025-17399-y · Cited by 1
In vivo metabolomics identifies CD38 as an emergent vulnerability in LKB1 -mutant lung cancerPreprint
Deng, J., Peng, D. H., Fenyö, D., Yuan, H., Lopez, A., Levin, D. S., Meynardie, M., Quinteros, M., Ranieri, M., Sahu, S., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.18.537350 · Cited by 4
Self-citationLee, M. W., Park, J. M., Cho, I. R., Chung, K. H., Choi, J. H., Paik, W. H., Ryu, J. K., Kim, B. S., Han, K., & Lee, S. H. (2025) · medRxiv · doi:10.1101/2025.03.11.25323676 · Cited by 1
Li, D., Roeck, K., Zhang, C., Zidek, B., Rodman, E. P. B., Hernandez-Barco, Y. G., Zhang, J., Bamlet, W. R., Oberg, A. L., Zhang, L., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.14.202952
Self-citationMunir, S., Ahmad, S., & Gul, A. (2021) · Preprints.org · doi:10.20944/preprints202102.0107.v1
Squamous Cell Carcinoma of the Lung in McCune-Albright Syndrome
Reddy, V. Y., Tvedten, E. J., & Louis, M. (2021) · Cureus · doi:10.7759/cureus.14159
Genomic medicine for the early detection of pancreatic cancer
Sato, H., Takahashi, K., & Mizukami, Y. (2022) · Suizo · doi:10.2958/suizo.37.29
Self-citationVuori, K., & Zhao, M. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736274644.793566082
(2023) · American Registry of PathologyArlington, Virginia eBooks · doi:10.55418/9781933477275-06
Wang, S., li, Y., Deng, J. K., Zhong, Y., Deng, J., Deng, L., Li, D., Feng, H., wang, Y., & Cao, H. (2024) · Research Square · doi:10.21203/rs.3.rs-4687848/v1
Pankaj, A., Raabe, M. J., Zhang, M. L., Song, Y., Patel, B. K., Xu, K., Kocher, J. R., Lang, E., Richieri, P., Caldwell, N. J., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.14.632658
Self-citationZoi, I., Rajput, M., Holguín-Horcajo, A., Haidar, M., Brusa, D., Chu, K., Xie, J., Shields, M. A., Ferreira, S., Stanger, B. Z., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.07.642043
Dual Role of NRF2 in Pancreatic Precursor Lesions
Ichimiya, S., Ahn, S. S., Dixon, M. S., O'Sullivan, J. P., DeVine, L., Chen, A., Yamamoto, T., Oda, Y., Nakamura, M., & Chio, I. I. C. (2025) · Cancer Research Communications · doi:10.1158/2767-9764.crc-25-0107
Loss of HNF1B drives pancreatic Intraductal Papillary and Mucinous Neoplasms (IPMN) initiationPreprint
Lorenzo, D., Munoz, L. A., MARSTRAND-DAUCE, L., Chassac, A., Nicole, P., Meng, L., Heidet, L., Knebelmann, B., Pignolet, C., Doblas, S., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.12.659269
Zhou, Y., Chen, L., Li, J., Zhang, H., Xiao, Y., Cai, Y., Wang, H., Zhen, Y., Liang, Z., & Shi, X. (2025) · Pathology - Research and Practice · doi:10.1016/j.prp.2025.156165
Expression and Clinical Significance of the GNAS Gene in Gastric Cancer
张, 尧. (2025) · Advances in Clinical Medicine · doi:10.12677/acm.2025.1582396
Chen, L., Peng, C., Chai, L., Zhang, R., Zhu, C., Wang, H., Cheng, Q., Yan, Y., Shen, C., Zheng, H., et al. (2025) · The EMBO Journal · doi:10.1038/s44318-025-00553-7
Sato, T., & Kato, Y. (2025) · Cureus · doi:10.7759/cureus.93715
Self-citationHou, P., Su, X., Cao, W., Xu, L., Zhang, R., Huang, Z., Wang, J., Li, L., Wu, L., & Liao, W. (2021) · Figshare · doi:10.6084/m9.figshare.14391217
Kong, G., Chen, L., Zhang, Q., Pan, J., & Liu, K. (2026) · Cellular Signalling · doi:10.1016/j.cellsig.2026.112407
Ruze, R., Tuerxun, R., Jiang, T., Aji, Y. S. A. T., & Aji, T. (2026) · IntechOpen eBooks · doi:10.5772/intechopen.1014946
Apport de l'ADN circulant tumoral dans les cancers digestifs
Evrard, C. (2022) · theses.fr (ABES) · doi:10.70675/e887f785zd2daz4c33za83fzd8d4cd2f9935
Lorenzo, D. (2024) · theses.fr (ABES) · doi:10.70675/ba1107b2ze1c9z4e6ezad24z3a1778a18d7e
Mandloi, A., Larson, C. R., Tran, T. M., Roy, S., Khaliq, A. M., Fang, Y.-H. D., Baines, J., Laube, R., Patel, M., Risley, C. A., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.27.728281
Hamada, T., Oyama, H., Nakai, Y., & Petrov, M. S. (2026) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djag225
Propionyl-CoA catabolism is a metabolic gatekeeper for fatty acid oxidation in pancreatic cancer
Yu, W., Wang, B., Meng, F., Ren, X., Zhou, D., Wei, H., Yang, Z., Sun, H., Jiang, M., Xia, T., et al. (2026) · Oncogene · doi:10.1038/s41388-026-03979-3
Hagedorn, G. A., Spieser, J., Hirai, N., Sato, Y., Valentine, J., Jiang, H., Wang, W., Czyzyk-Krzeska, M., & Patra, K. C. (2026) · Science Advances · doi:10.1126/sciadv.aeh7186
Self-citation
Metadata
- Authors
- Patra, K. C., Kato, Y., Mizukami, Y., Widholz, S., Boukhali, M., Revenco, I., Grossman, E. A., Ji, F., Sadreyev, R. I., Liss, A. S., Screaton, R. A., Sakamoto, K., Ryan, D. P., Mino-Kenudson, M., Castillo, C. F.-D., Nomura, D. K., Haas, W., & Bardeesy, N.
- Affiliations
- Harvard University (US)
- Massachusetts General Hospital (US)
- Asahikawa Medical University (JP)
- University of California, Berkeley (US)
- University of Toronto (CA)
- University of Dundee (GB)
- Corresponding author
- Bardeesy, Nabeel
- ORCID
- Venue
- Nature Cell Biology
- Published
- 2018-06-25
- Volume
- 20
- Issue
- 7
- Pages
- 811-822
- ISSN
- 1465-7392 (ISSN-L)
- 1476-4679
- PMC
- PMC6044476
- OpenAlex
- W2809279418
- Cited by
- 192
- References
- 70
- Citations by year
- 2026: 10 · 2025: 35 · 2024: 31 · 2023: 29 · 2022: 21 · 2021: 28 · 2020: 14 · 2019: 19 · 2018: 5
- FWCI
- 6.19
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Japan Society for the Promotion of Science (17K09472)
- National Cancer Institute (P50CA127003, R01CA133557, P01CA117969)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK040561)
- Topics
- Health Sciences › Medicine › Oncology › Pancreatic and Hepatic Oncology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Lipids, and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Keywords
- GNAS, pancreatic ductal adenocarcinoma, intraductal papillary mucinous neoplasm, KRAS G12D, cAMP signaling, protein kinase A, salt-inducible kinases, lipid remodeling, fatty acid oxidation, cancer metabolism, p53 deficiency, tumour suppressor, oncogenic mechanisms
- MeSH terms
- Animals, Cell Transformation, Neoplastic, Chromogranins, Enzyme Repression, Fatty Acids, Female, Humans, Male, Mice, Inbred C57BL, Mice, Mutant Strains, Mice, Transgenic, Mutation, Oxidation-Reduction, Pancreatic Neoplasms, Phenotype, Genes, ras, Time Factors, Tumor Cells, Cultured, Signal Transduction, Gene Expression Regulation, Neoplastic, Tumor Suppressor Protein p53, Mice, Inbred NOD, Protein Serine-Threonine Kinases, Cyclic AMP-Dependent Protein Kinases, GTP-Binding Protein alpha Subunits, Gs, Genetic Predisposition to Disease, Carcinoma, Pancreatic Ductal, Cell Line, Tumor, Lipid Metabolism, Mice, 129 Strain, Cellular Reprogramming
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review