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Abstract 2090: TP73 expression may be influenced by DNA methylation in human tumorigenesis 摘要:TP73的表达可能受到DNA甲基化在人类肿瘤发生中的影响
Molecular and Cellular Biology / Genetics Pub Date : 2021-07-01 DOI: 10.1158/1538-7445.AM2021-2090
Z. Yao, D. Yao, William W. Yu, A. Malki, Z. Sherif
{"title":"Abstract 2090: TP73 expression may be influenced by DNA methylation in human tumorigenesis","authors":"Z. Yao, D. Yao, William W. Yu, A. Malki, Z. Sherif","doi":"10.1158/1538-7445.AM2021-2090","DOIUrl":"https://doi.org/10.1158/1538-7445.AM2021-2090","url":null,"abstract":"","PeriodicalId":18754,"journal":{"name":"Molecular and Cellular Biology / Genetics","volume":"1121 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91444314","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Abstract 2021: Differential expression of antioxidant and detoxifying enzymes induced by e-cigarette aerosol 2021:电子烟气雾剂诱导抗氧化和解毒酶的差异表达
Molecular and Cellular Biology / Genetics Pub Date : 2021-07-01 DOI: 10.1158/1538-7445.AM2021-2021
Vengatesh Ganapathy, Jimmy Manyanga, L. Queimado
{"title":"Abstract 2021: Differential expression of antioxidant and detoxifying enzymes induced by e-cigarette aerosol","authors":"Vengatesh Ganapathy, Jimmy Manyanga, L. Queimado","doi":"10.1158/1538-7445.AM2021-2021","DOIUrl":"https://doi.org/10.1158/1538-7445.AM2021-2021","url":null,"abstract":"Background The BioFire FilmArrary GI Panel Assay is a highly sensitive PCR-based diagnostic test capable of detecting 22 different gastrointestinal pathogens from stool specimens. The predominant pathogens associated with hospital-acquired gastroenteritis are Clostridioides difficile and Norovirus, both of which can be assayed individually with PCR-based tests performed at UCHealth. Previous studies favor a cost-saving ‘3-day rule,’ that restricts ordering culture-based stool testing on inpatient adults following the 3rd day of hospitalization. However, the previous studies performed a limited analysis of pathogens using predominantly culture-based assays. Furthermore certain patient groups may be at high risk for developing nosocomial diarrhea with less common organisms, which may go undetected if the 3-day rule were enforced for the GI panel assay. Thus there is a need to validate whether the 3-day rule is appropriate for restricting the use of the GI panel assay for the evaluation of nosocomial diarrhea.","PeriodicalId":18754,"journal":{"name":"Molecular and Cellular Biology / Genetics","volume":"11 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80765477","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Abstract 2416: Upregulation of amplified in breast cancer 1 contributes to pancreatic ductal adenocarcinoma progression and vulnerability to blockage of hedgehog activation 2416:在乳腺癌中扩增1的上调有助于胰腺导管腺癌的进展和对hedgehog激活阻断的易感性
Molecular and Cellular Biology / Genetics Pub Date : 2021-07-01 DOI: 10.1158/1538-7445.AM2021-2416
Licen Li, Jiaolin Bao, Haitao Wang, Haipeng Lei, P.-T. Cheng, Jianming Zeng, Wenhui Hao, Xu Zhang, Xiaoling Xu, Chundong Yu, C. Deng, Qiang Chen
{"title":"Abstract 2416: Upregulation of amplified in breast cancer 1 contributes to pancreatic ductal adenocarcinoma progression and vulnerability to blockage of hedgehog activation","authors":"Licen Li, Jiaolin Bao, Haitao Wang, Haipeng Lei, P.-T. Cheng, Jianming Zeng, Wenhui Hao, Xu Zhang, Xiaoling Xu, Chundong Yu, C. Deng, Qiang Chen","doi":"10.1158/1538-7445.AM2021-2416","DOIUrl":"https://doi.org/10.1158/1538-7445.AM2021-2416","url":null,"abstract":"Background: Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive and devastating cancers without effective treatments. Amplified in breast cancer 1 (AIB1) is a member of the steroid receptor coactivator family that mediates the transcriptional activities of nuclear receptors. While AIB1 is associated with the initiation and progression of multiple cancers, the mechanism by which AIB1 contributes to PDAC progression remains largely unknown. In this study, we aimed to explore the role of AIB1 in the progression of PDAC and elucidate the underlying mechanisms. Methods: The clinical significance and mRNA level of AIB1 in PDAC were studied by database analysis. To demonstrate whether AIB1 mediates the malignant features of PDAC cells, namely, proliferation, migration, invasion, we performed real-time PCR and Western blot analysis, established xenograft models and used in vivo metastasis assay. With insights into the mechanism of AIB1, we performed RNA sequencing (Seq), ChIP-Seq, luciferase reporter assays and pull-down assays. Furthermore, we analyzed the relationship between AIB1 expression and its target expression in PDAC cells and patients and explored whether PDAC cells with high AIB1 levels are sensitive to inhibitors of its target. Results: We found that AIB1 was significantly upregulated in PDAC and associated with its malignancy. Silencing AIB1 impaired hedgehog (Hh) activation by reducing the expression of smoothened (SMO), leading to cell cycle arrest and the inhibition of PDAC cell proliferation. In addition, AIB1, via upregulation of integrin αv (ITGAV) expression, promoted extracellular matrix (ECM) signaling, which played an important role in PDAC progression. Further studies showed that AIB1 preferably bound to AP-1 related elements and served as a coactivator for enhancing the transcriptional activity of MafB, which promoted the expression of SMO and ITGAV. PDAC cells with high AIB1 levels were sensitive to Hh signaling inhibitors, suggesting that blocking Hh activation is an effective treatment against PDAC with high AIB1 expression. Conclusions: These findings reveal that AIB1 is a crucial oncogenic regulator associated with PDAC progression via Hh and ECM signaling and suggest potential therapeutic targets for PDAC treatment. Citation Format: Licen Li, Jiaolin Bao, Haitao Wang, Haipeng Lei, Peng Cheng, Jianming Zeng, Wenhui Hao, Xu Zhang, Xiaoling Xu, Chundong Yu, Chu-Xia Deng, Qiang Chen. Upregulation of amplified in breast cancer 1 contributes to pancreatic ductal adenocarcinoma progression and vulnerability to blockage of hedgehog activation [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2416.","PeriodicalId":18754,"journal":{"name":"Molecular and Cellular Biology / Genetics","volume":"43 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83758251","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Abstract 2466: Stochastic loss of GLUL expression correlates with STK11-loss-dependent glutamine addiction and may impact anti-PD1 therapy resistance in NSCLC 2466: GLUL表达的随机缺失与stk11缺失依赖的谷氨酰胺成瘾相关,并可能影响NSCLC的抗pd1治疗耐药性
Molecular and Cellular Biology / Genetics Pub Date : 2021-07-01 DOI: 10.1158/1538-7445.AM2021-2466
Sean M. Lenahan, Hailey M. Sarausky, D. Seward
{"title":"Abstract 2466: Stochastic loss of GLUL expression correlates with STK11-loss-dependent glutamine addiction and may impact anti-PD1 therapy resistance in NSCLC","authors":"Sean M. Lenahan, Hailey M. Sarausky, D. Seward","doi":"10.1158/1538-7445.AM2021-2466","DOIUrl":"https://doi.org/10.1158/1538-7445.AM2021-2466","url":null,"abstract":"","PeriodicalId":18754,"journal":{"name":"Molecular and Cellular Biology / Genetics","volume":"6 6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81033588","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Abstract 2377: microRNA expression profile in urinary exosomes is dependent on non-invasive lymphoma induction in mice 摘要2377:小鼠尿外泌体中的microRNA表达谱依赖于非侵袭性淋巴瘤诱导
Molecular and Cellular Biology / Genetics Pub Date : 2021-07-01 DOI: 10.1158/1538-7445.AM2021-2377
B. Wilson, Rebekah Betar, Alexander Martin, Z. Niazi, Michael P. Boyer, Lori Winter, V. Babich, F. Sole, E. Ananieva
{"title":"Abstract 2377: microRNA expression profile in urinary exosomes is dependent on non-invasive lymphoma induction in mice","authors":"B. Wilson, Rebekah Betar, Alexander Martin, Z. Niazi, Michael P. Boyer, Lori Winter, V. Babich, F. Sole, E. Ananieva","doi":"10.1158/1538-7445.AM2021-2377","DOIUrl":"https://doi.org/10.1158/1538-7445.AM2021-2377","url":null,"abstract":"Lymphoma accounts for approximately 4% of cancers in the United States, with an estimated 20,910 number of deaths per year. The standard method of diagnosis and staging of lymphoma involves surgical biopsy of the tumor - a procedure that has many negative associated risks. Exosomes are extracellular vesicles secreted in biological fluids that can serve as “liquid biomarkers”. Identification of unique cancer-related biomarkers in urinary exosomes may provide a novel non-invasive and cost-effective tool for lymphoma diagnosis. Analyses of biomarkers obtained from urinary exosomes have been used to evaluate urological cancers, however, these methods have not yet been translated to non-urological pathologies, such as lymphomas. The objective for this study was to determine the profile of microRNAs (miRNAs) expressed in urinary exosomes of mice challenged with lymphoma and compare it to miRNAs identified in urinary exosomes of control mice. Male and female C57BL/6 mice, (tumor (+), n=12), were injected with either 2.5x105 mouse EL-4 lymphoma cells or phosphate-buffered saline (tumor (-), n=12). Tumor growth was monitored for 20 days. Urine was collected for 48 hours starting on day 17 and serum, tumor tissues, and organs were collected on day 20. Extraction of urinary exosomes was followed by total RNA isolation and RT-qPCR for which a set of PCR arrays consisting of 709 mouse-specific miRNA primers was used. Fold changes in miRNA expression were quantified using the ΔΔCt method. Mice developed tumors by day 13 with initial tumor appearance around day seven. There were no statistically significant differences between final tumor mass, body weight, or food and water intake in tumor (+) versus tumor (-) mice. RT-qPCR arrays of miRNAs extracted from urinary exosomes revealed 464 miRNAs that were differentially expressed between tumor (+) and tumor (-). 215 miRNAs were up-regulated, while 249 miRNAs were down-regulated in tumor (+) mice. These results will be compared to miRNAs from serum and tumor tissues to identify tumor-specific miRNAs that can be used for potential application in the clinical setting. Citation Format: Brittany Wilson, Rebekah Betar, Alexander Martin, Zackaria Niazi, Michael Boyer, Lori Winter, Victor Babich, Francesca Di Sole, Elitsa Ananieva. microRNA expression profile in urinary exosomes is dependent on non-invasive lymphoma induction in mice [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2377.","PeriodicalId":18754,"journal":{"name":"Molecular and Cellular Biology / Genetics","volume":"18 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89366780","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Abstract 2400: PINK1 is a novel regulator of mitochondria and iron metabolism in colon cancer 摘要2400:PINK1是结肠癌线粒体和铁代谢的新调控因子
Molecular and Cellular Biology / Genetics Pub Date : 2021-07-01 DOI: 10.1158/1538-7445.AM2021-2400
Brandon Chen, S. Devenport, C. Lyssiotis, Y. Shah
{"title":"Abstract 2400: PINK1 is a novel regulator of mitochondria and iron metabolism in colon cancer","authors":"Brandon Chen, S. Devenport, C. Lyssiotis, Y. Shah","doi":"10.1158/1538-7445.AM2021-2400","DOIUrl":"https://doi.org/10.1158/1538-7445.AM2021-2400","url":null,"abstract":"","PeriodicalId":18754,"journal":{"name":"Molecular and Cellular Biology / Genetics","volume":"27 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87232155","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Abstract 2046: Binding of FANCD2 to SRSF1 splicing factor prevents genomic instability through R-loop regulation 2046: FANCD2与SRSF1剪接因子的结合通过R-loop调控防止基因组不稳定
Molecular and Cellular Biology / Genetics Pub Date : 2021-07-01 DOI: 10.1158/1538-7445.AM2021-2046
Anne Olazabal-Herrero, Allison M. Green, Xiaoyong Chen, P. Sung, Pillai M. Manoj, G. Kupfer
{"title":"Abstract 2046: Binding of FANCD2 to SRSF1 splicing factor prevents genomic instability through R-loop regulation","authors":"Anne Olazabal-Herrero, Allison M. Green, Xiaoyong Chen, P. Sung, Pillai M. Manoj, G. Kupfer","doi":"10.1158/1538-7445.AM2021-2046","DOIUrl":"https://doi.org/10.1158/1538-7445.AM2021-2046","url":null,"abstract":"","PeriodicalId":18754,"journal":{"name":"Molecular and Cellular Biology / Genetics","volume":"74 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90601714","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Abstract 2153:KRT16andE6-E7HR-HPV mRNAin situexpression in normal cervical tissue, and low-grade and high-grade squamous intraepithelial lesions 2153: krt16和de6 - e7hr - hpv mRNAin在正常宫颈组织、低级别和高级别鳞状上皮内病变中的表达
Molecular and Cellular Biology / Genetics Pub Date : 2021-07-01 DOI: 10.1158/1538-7445.AM2021-2153
Ines Benedetti, Reinhard Rodríguez, Lía Barrios
{"title":"Abstract 2153:KRT16andE6-E7HR-HPV mRNAin situexpression in normal cervical tissue, and low-grade and high-grade squamous intraepithelial lesions","authors":"Ines Benedetti, Reinhard Rodríguez, Lía Barrios","doi":"10.1158/1538-7445.AM2021-2153","DOIUrl":"https://doi.org/10.1158/1538-7445.AM2021-2153","url":null,"abstract":"","PeriodicalId":18754,"journal":{"name":"Molecular and Cellular Biology / Genetics","volume":"53 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80668585","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Abstract 2244: Evaluation of large antibody panels in single-cell genomic immunophenotyping of fresh and preserved human leukocytes 摘要:大抗体板在新鲜和保存的人白细胞单细胞基因组免疫表型分析中的评价
Molecular and Cellular Biology / Genetics Pub Date : 2021-07-01 DOI: 10.1158/1538-7445.AM2021-2244
N. Siemers, Jasmine Chen, P. Mankoo, S. Ilyas
{"title":"Abstract 2244: Evaluation of large antibody panels in single-cell genomic immunophenotyping of fresh and preserved human leukocytes","authors":"N. Siemers, Jasmine Chen, P. Mankoo, S. Ilyas","doi":"10.1158/1538-7445.AM2021-2244","DOIUrl":"https://doi.org/10.1158/1538-7445.AM2021-2244","url":null,"abstract":"","PeriodicalId":18754,"journal":{"name":"Molecular and Cellular Biology / Genetics","volume":"19 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86953525","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Abstract 2233: Landscape of driver mutations in MAPK/PI3K/AKT signaling pathways reveals insights into therapeutic targeting strategies 摘要:MAPK/PI3K/AKT信号通路的驱动突变揭示了治疗靶向策略的见解
Molecular and Cellular Biology / Genetics Pub Date : 2021-07-01 DOI: 10.1158/1538-7445.AM2021-2233
S. Sivakumar, E. Sokol, G. Frampton, P. Hegde, D. Fabrizio
{"title":"Abstract 2233: Landscape of driver mutations in MAPK/PI3K/AKT signaling pathways reveals insights into therapeutic targeting strategies","authors":"S. Sivakumar, E. Sokol, G. Frampton, P. Hegde, D. Fabrizio","doi":"10.1158/1538-7445.AM2021-2233","DOIUrl":"https://doi.org/10.1158/1538-7445.AM2021-2233","url":null,"abstract":"","PeriodicalId":18754,"journal":{"name":"Molecular and Cellular Biology / Genetics","volume":"346 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79667395","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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