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Molecular and Cellular Oncology最新文献

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Complex interplay between p53 and chromosome stability. p53与染色体稳定性之间的复杂相互作用。
IF 2.1
Molecular and Cellular Oncology Pub Date : 2021-06-28 eCollection Date: 2021-01-01 DOI: 10.1080/23723556.2021.1938479
Akshay Narkar, Blake A Johnson, Rong Li
{"title":"Complex interplay between p53 and chromosome stability.","authors":"Akshay Narkar,&nbsp;Blake A Johnson,&nbsp;Rong Li","doi":"10.1080/23723556.2021.1938479","DOIUrl":"https://doi.org/10.1080/23723556.2021.1938479","url":null,"abstract":"<p><p>TP53-dependent cell cycle arrest has been proposed to limit the proliferation of aneuploid cells. We investigated the cellular response to aneuploidy in cell lines and organoid cultures and found that TP53 (also known as p53) is not activated following aneuploidy induction in organoids. However, we confirmed that p53 is required for high mitotic fidelity. Our findings provide a revised view on how p53 safeguards against aneuploidy.</p>","PeriodicalId":37292,"journal":{"name":"Molecular and Cellular Oncology","volume":"8 4","pages":"1938479"},"PeriodicalIF":2.1,"publicationDate":"2021-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23723556.2021.1938479","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39492058","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Combining VEGF receptor inhibitors and angiotensin-(1-7) to target renal cell carcinoma. 联合VEGF受体抑制剂和血管紧张素-(1-7)治疗肾细胞癌。
IF 2.1
Molecular and Cellular Oncology Pub Date : 2021-06-12 eCollection Date: 2021-01-01 DOI: 10.1080/23723556.2021.1918529
Thomas Walther, Prateek Khanna, Rupal S Bhatt
{"title":"Combining VEGF receptor inhibitors and angiotensin-(1-7) to target renal cell carcinoma.","authors":"Thomas Walther,&nbsp;Prateek Khanna,&nbsp;Rupal S Bhatt","doi":"10.1080/23723556.2021.1918529","DOIUrl":"https://doi.org/10.1080/23723556.2021.1918529","url":null,"abstract":"<p><p>Resistance to tyrosine kinase inhibitors of the vascular endothelial growth factor receptor inevitably develops in most patients with metastatic kidney cancer. Our recent findings demonstrate that addition of angiotensin-(1-7) peptide can be a potential therapy that delays such resistance.</p>","PeriodicalId":37292,"journal":{"name":"Molecular and Cellular Oncology","volume":"8 4","pages":"1918529"},"PeriodicalIF":2.1,"publicationDate":"2021-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23723556.2021.1918529","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39492051","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Regulation of glycolysis and cancer cell proliferation by PKM2 citrullination. PKM2瓜氨酸化对糖酵解和癌细胞增殖的调控。
IF 2.1
Molecular and Cellular Oncology Pub Date : 2021-06-04 eCollection Date: 2021-01-01 DOI: 10.1080/23723556.2021.1927446
Sébastien Coassolo, Irwin Davidson
{"title":"Regulation of glycolysis and cancer cell proliferation by PKM2 citrullination.","authors":"Sébastien Coassolo,&nbsp;Irwin Davidson","doi":"10.1080/23723556.2021.1927446","DOIUrl":"https://doi.org/10.1080/23723556.2021.1927446","url":null,"abstract":"<p><p>Conversion of peptidyl-arginine to peptidyl citrulline, known as citrullination, is a post-translational protein modification catalyzed by the PADI (Protein Arginine Deiminase) family of enzymes. PADI1 and PADI3 catalyze citrullination of arginine 106 in the glycolytic enzyme pyruvate kinase M2 modulating its allosteric regulation, glycolysis and cancer cell proliferation.</p>","PeriodicalId":37292,"journal":{"name":"Molecular and Cellular Oncology","volume":"8 4","pages":"1927446"},"PeriodicalIF":2.1,"publicationDate":"2021-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23723556.2021.1927446","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39492054","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
The concerted action of oncogenic driver mutations directs global translation in intestinal epithelial cells. 致癌驱动突变的协同作用指导肠上皮细胞的全局翻译。
IF 2.1
Molecular and Cellular Oncology Pub Date : 2021-05-19 eCollection Date: 2021-01-01 DOI: 10.1080/23723556.2021.1879614
Wouter Smit, Jarom Heijmans
{"title":"The concerted action of oncogenic driver mutations directs global translation in intestinal epithelial cells.","authors":"Wouter Smit,&nbsp;Jarom Heijmans","doi":"10.1080/23723556.2021.1879614","DOIUrl":"https://doi.org/10.1080/23723556.2021.1879614","url":null,"abstract":"<p><p>Oncogenic transformation of colorectal cancer cells is driven by a set of mutations that cause aberrant signaling of growth factor-receptor pathways. Using organoids, we demonstrate that the most frequent driver mutations in <i>APC, KRAS, SMAD4</i>, and <i>TP53</i> are enhancers of the global mRNA translational capacity, which is linked to intestinal cell growth in an mTOR-dependent manner.</p>","PeriodicalId":37292,"journal":{"name":"Molecular and Cellular Oncology","volume":"8 4","pages":"1879614"},"PeriodicalIF":2.1,"publicationDate":"2021-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23723556.2021.1879614","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39492050","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Yes, MAM! 是的,老妈!
IF 2.1
Molecular and Cellular Oncology Pub Date : 2021-05-19 eCollection Date: 2021-01-01 DOI: 10.1080/23723556.2021.1919473
Robert E Means, Samuel G Katz
{"title":"Yes, MAM!","authors":"Robert E Means,&nbsp;Samuel G Katz","doi":"10.1080/23723556.2021.1919473","DOIUrl":"https://doi.org/10.1080/23723556.2021.1919473","url":null,"abstract":"<p><p>Regulation of cell life and death by members of the BCL-2 family of proteins occurs at the mitochondria. Large portions of the mitochondria's outer membrane are found in tight approximation with the endoplasmic reticulum (ER), known as mitochondria-associated membranes (MAMs) or mitochondria-ER contact sites (MERCs). We recently reported that BOK is present within MAMs where it regulates Ca<sup>2+</sup> transfer from the ER to the mitochondria, appropriate MAM components and MERC structure, and apoptosis.</p>","PeriodicalId":37292,"journal":{"name":"Molecular and Cellular Oncology","volume":"8 4","pages":"1919473"},"PeriodicalIF":2.1,"publicationDate":"2021-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23723556.2021.1919473","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39492052","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 9
Regulation of nuclear mTORC1. 核mTORC1的调控。
IF 2.1
Molecular and Cellular Oncology Pub Date : 2021-05-05 eCollection Date: 2021-01-01 DOI: 10.1080/23723556.2021.1896348
Xin Zhou, Yanghao Zhong, Jin Zhang
{"title":"Regulation of nuclear mTORC1.","authors":"Xin Zhou,&nbsp;Yanghao Zhong,&nbsp;Jin Zhang","doi":"10.1080/23723556.2021.1896348","DOIUrl":"https://doi.org/10.1080/23723556.2021.1896348","url":null,"abstract":"<p><p>mTORC1 integrates diverse upstream signals to control cell growth and metabolism. We previously showed that mTORC1 activity is spatially compartmentalized to ensure its signaling specificity. In a recently published study, we demonstrated the existence of mTORC1 activity in the nucleus and identified a unique mode of its regulation in the nuclear compartment.</p>","PeriodicalId":37292,"journal":{"name":"Molecular and Cellular Oncology","volume":"8 3","pages":"1896348"},"PeriodicalIF":2.1,"publicationDate":"2021-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23723556.2021.1896348","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39010559","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Regulation of autophagy by VPS34 branched ubiquitination controls proteostasis and liver metabolism. VPS34支链泛素化对自噬的调控控制着蛋白质稳态和肝脏代谢。
IF 2.1
Molecular and Cellular Oncology Pub Date : 2021-05-05 eCollection Date: 2021-01-01 DOI: 10.1080/23723556.2021.1915076
Yu-Hsuan Chen, Ruey-Hwa Chen
{"title":"Regulation of autophagy by VPS34 branched ubiquitination controls proteostasis and liver metabolism.","authors":"Yu-Hsuan Chen,&nbsp;Ruey-Hwa Chen","doi":"10.1080/23723556.2021.1915076","DOIUrl":"https://doi.org/10.1080/23723556.2021.1915076","url":null,"abstract":"<p><p>Ubiquitin-proteasome system and autophagy are the two major recycling processes. Our recent work uncovers a K29/K48 branched ubiquitination on the phosphatidylinositol 3-kinase catalytic subunit type 3 (PI3KC3, best known as VPS34). This ubiquitination is positively or negatively regulated under pathophysiological conditions to influence on autophagy, proteostasis and lipid homeostasis.</p>","PeriodicalId":37292,"journal":{"name":"Molecular and Cellular Oncology","volume":"8 3","pages":"1915076"},"PeriodicalIF":2.1,"publicationDate":"2021-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23723556.2021.1915076","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39012049","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
FOXA1 mutations influence the therapeutic response of breast cancer by altering chromatin state. FOXA1突变通过改变染色质状态影响乳腺癌的治疗反应。
IF 2.1
Molecular and Cellular Oncology Pub Date : 2021-05-05 eCollection Date: 2021-01-01 DOI: 10.1080/23723556.2021.1891831
Amaia Arruabarrena-Aristorena, Eneda Toska
{"title":"<i>FOXA1</i> mutations influence the therapeutic response of breast cancer by altering chromatin state.","authors":"Amaia Arruabarrena-Aristorena,&nbsp;Eneda Toska","doi":"10.1080/23723556.2021.1891831","DOIUrl":"https://doi.org/10.1080/23723556.2021.1891831","url":null,"abstract":"ABSTRACT Forkhead box protein A1 (FOXA1) is a pioneer transcription factor that contributes to chromatin opening to allow binding of estrogen receptor (ER) in ER+ breast cancer. Mutations in FOXA1 are recurrent in breast cancer but the functional consequences of these mutations remain unknown. We identified that FOXA1 mutations are associated with worse outcomes to endocrine therapy by inducing alternative chromatin profiles and gene activity in breast cancer.","PeriodicalId":37292,"journal":{"name":"Molecular and Cellular Oncology","volume":"8 3","pages":"1891831"},"PeriodicalIF":2.1,"publicationDate":"2021-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23723556.2021.1891831","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39010557","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The importance of transmembrane domain interactions in the viral control of apoptosis. 跨膜结构域相互作用在病毒控制细胞凋亡中的重要性。
IF 2.1
Molecular and Cellular Oncology Pub Date : 2021-05-03 eCollection Date: 2021-01-01 DOI: 10.1080/23723556.2021.1911290
Gerard Duart, Ismael Mingarro, Luis Martinez-Gil
{"title":"The importance of transmembrane domain interactions in the viral control of apoptosis.","authors":"Gerard Duart,&nbsp;Ismael Mingarro,&nbsp;Luis Martinez-Gil","doi":"10.1080/23723556.2021.1911290","DOIUrl":"https://doi.org/10.1080/23723556.2021.1911290","url":null,"abstract":"<p><p>Viral control of apoptosis occurs through the expression of viral encoded anti-apoptotic B-cell lymphoma 2 (BCL2) analogs. These proteins are thought to restrain apoptosis by interacting with cellular BCL2 family members. We identified that protein-protein interactions between cellular and viral BCL2 transmembrane domains are crucial for the viral protein's function.</p>","PeriodicalId":37292,"journal":{"name":"Molecular and Cellular Oncology","volume":"8 3","pages":"1911290"},"PeriodicalIF":2.1,"publicationDate":"2021-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23723556.2021.1911290","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39012046","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Zmat3 splices together p53-dependent tumor suppression. Zmat3拼接在一起p53依赖性肿瘤抑制。
IF 2.1
Molecular and Cellular Oncology Pub Date : 2021-04-29 eCollection Date: 2021-01-01 DOI: 10.1080/23723556.2021.1898523
Kathryn T Bieging-Rolett, Laura D Attardi
{"title":"Zmat3 splices together p53-dependent tumor suppression.","authors":"Kathryn T Bieging-Rolett,&nbsp;Laura D Attardi","doi":"10.1080/23723556.2021.1898523","DOIUrl":"https://doi.org/10.1080/23723556.2021.1898523","url":null,"abstract":"<p><p>The tumor protein p53 (TP53, best known as p53) transcription factor is a critical tumor suppressor, but those p53-inducible genes most important for tumor suppression have remained unclear. Using unbiased RNA interference and CRISPR (Clustered Regularly Interspersed Palindromic Repeats)/Cas9 (CRISPR-associated protein 9) screens, genetically engineered mouse models, human cancer genome analysis, and integrative eCLIP-sequencing and RNA-sequencing analyses, we reveal a new branch of p53-mediated tumor suppression involving the RNA splicing regulator Zinc finger Matrin-type 3, Zmat3.</p>","PeriodicalId":37292,"journal":{"name":"Molecular and Cellular Oncology","volume":"8 3","pages":"1898523"},"PeriodicalIF":2.1,"publicationDate":"2021-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23723556.2021.1898523","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39010561","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
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