Celecoxib increases miR-222 while deterring aromatase-expressing breast tumor growth in mice

10.1186/1471-2407-14-426

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Main Authors:	Wong, T.Y, Li, F, Lin, S.-M, Chan, F.L, Chen, S, Leung, L.K
Other Authors:	DUKE-NUS MEDICAL SCHOOL
Format:	Article
Published:	2020
Subjects:	acetylsalicylic acid androstenedione aromatase celecoxib cyclin A cyclooxygenase 2 estradiol estrogen receptor alpha messenger RNA microRNA 222 Myc protein protein bcl xl transcription factor E2F2 cyclooxygenase 2 inhibitor microRNA MIRN222 microRNA, human pyrazole derivative sulfonamide animal experiment animal model animal tissue article body weight breast tumor controlled study down regulation estradiol blood level female liver weight MCF 7 cell line mouse nonhuman nude mouse protein expression tumor growth tumor xenograft anatomy and histology animal apoptosis blood cell cycle disease model drug effects drug screening gene expression regulation genetics human liver metabolism oncogene myc pathology tumor volume Animals Apoptosis Aromatase Aspirin Body Weight Breast Neoplasms Cell Cycle Cyclooxygenase 2 Cyclooxygenase 2 Inhibitors Disease Models, Animal E2F2 Transcription Factor Estradiol Estrogen Receptor alpha Female Gene Expression Regulation, Neoplastic Genes, myc Humans Liver MCF-7 Cells Mice MicroRNAs Pyrazoles RNA, Messenger Sulfonamides Tumor Burden Xenograft Model Antitumor Assays
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/181498
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1814982023-11-01T07:35:58Z Celecoxib increases miR-222 while deterring aromatase-expressing breast tumor growth in mice Wong, T.Y Li, F Lin, S.-M Chan, F.L Chen, S Leung, L.K DUKE-NUS MEDICAL SCHOOL acetylsalicylic acid androstenedione aromatase celecoxib cyclin A cyclooxygenase 2 estradiol estrogen receptor alpha messenger RNA microRNA 222 Myc protein protein bcl xl transcription factor E2F2 acetylsalicylic acid aromatase celecoxib cyclooxygenase 2 cyclooxygenase 2 inhibitor estradiol estrogen receptor alpha messenger RNA microRNA MIRN222 microRNA, human pyrazole derivative sulfonamide transcription factor E2F2 animal experiment animal model animal tissue article body weight breast tumor controlled study down regulation estradiol blood level female liver weight MCF 7 cell line mouse nonhuman nude mouse protein expression tumor growth tumor xenograft anatomy and histology animal apoptosis blood breast tumor cell cycle disease model drug effects drug screening gene expression regulation genetics human liver metabolism oncogene myc pathology tumor volume Animals Apoptosis Aromatase Aspirin Body Weight Breast Neoplasms Cell Cycle Cyclooxygenase 2 Cyclooxygenase 2 Inhibitors Disease Models, Animal E2F2 Transcription Factor Estradiol Estrogen Receptor alpha Female Gene Expression Regulation, Neoplastic Genes, myc Humans Liver MCF-7 Cells Mice MicroRNAs Pyrazoles RNA, Messenger Sulfonamides Tumor Burden Xenograft Model Antitumor Assays 10.1186/1471-2407-14-426 BMC Cancer 14 1 426 2020-10-27T11:07:02Z 2020-10-27T11:07:02Z 2014 Article Wong, T.Y, Li, F, Lin, S.-M, Chan, F.L, Chen, S, Leung, L.K (2014). Celecoxib increases miR-222 while deterring aromatase-expressing breast tumor growth in mice. BMC Cancer 14 (1) : 426. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2407-14-426 14712407 https://scholarbank.nus.edu.sg/handle/10635/181498 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20201031
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	acetylsalicylic acid androstenedione aromatase celecoxib cyclin A cyclooxygenase 2 estradiol estrogen receptor alpha messenger RNA microRNA 222 Myc protein protein bcl xl transcription factor E2F2 acetylsalicylic acid aromatase celecoxib cyclooxygenase 2 cyclooxygenase 2 inhibitor estradiol estrogen receptor alpha messenger RNA microRNA MIRN222 microRNA, human pyrazole derivative sulfonamide transcription factor E2F2 animal experiment animal model animal tissue article body weight breast tumor controlled study down regulation estradiol blood level female liver weight MCF 7 cell line mouse nonhuman nude mouse protein expression tumor growth tumor xenograft anatomy and histology animal apoptosis blood breast tumor cell cycle disease model drug effects drug screening gene expression regulation genetics human liver metabolism oncogene myc pathology tumor volume Animals Apoptosis Aromatase Aspirin Body Weight Breast Neoplasms Cell Cycle Cyclooxygenase 2 Cyclooxygenase 2 Inhibitors Disease Models, Animal E2F2 Transcription Factor Estradiol Estrogen Receptor alpha Female Gene Expression Regulation, Neoplastic Genes, myc Humans Liver MCF-7 Cells Mice MicroRNAs Pyrazoles RNA, Messenger Sulfonamides Tumor Burden Xenograft Model Antitumor Assays
spellingShingle	acetylsalicylic acid androstenedione aromatase celecoxib cyclin A cyclooxygenase 2 estradiol estrogen receptor alpha messenger RNA microRNA 222 Myc protein protein bcl xl transcription factor E2F2 acetylsalicylic acid aromatase celecoxib cyclooxygenase 2 cyclooxygenase 2 inhibitor estradiol estrogen receptor alpha messenger RNA microRNA MIRN222 microRNA, human pyrazole derivative sulfonamide transcription factor E2F2 animal experiment animal model animal tissue article body weight breast tumor controlled study down regulation estradiol blood level female liver weight MCF 7 cell line mouse nonhuman nude mouse protein expression tumor growth tumor xenograft anatomy and histology animal apoptosis blood breast tumor cell cycle disease model drug effects drug screening gene expression regulation genetics human liver metabolism oncogene myc pathology tumor volume Animals Apoptosis Aromatase Aspirin Body Weight Breast Neoplasms Cell Cycle Cyclooxygenase 2 Cyclooxygenase 2 Inhibitors Disease Models, Animal E2F2 Transcription Factor Estradiol Estrogen Receptor alpha Female Gene Expression Regulation, Neoplastic Genes, myc Humans Liver MCF-7 Cells Mice MicroRNAs Pyrazoles RNA, Messenger Sulfonamides Tumor Burden Xenograft Model Antitumor Assays Wong, T.Y Li, F Lin, S.-M Chan, F.L Chen, S Leung, L.K Celecoxib increases miR-222 while deterring aromatase-expressing breast tumor growth in mice
description	10.1186/1471-2407-14-426
author2	DUKE-NUS MEDICAL SCHOOL
author_facet	DUKE-NUS MEDICAL SCHOOL Wong, T.Y Li, F Lin, S.-M Chan, F.L Chen, S Leung, L.K
format	Article
author	Wong, T.Y Li, F Lin, S.-M Chan, F.L Chen, S Leung, L.K
author_sort	Wong, T.Y
title	Celecoxib increases miR-222 while deterring aromatase-expressing breast tumor growth in mice
title_short	Celecoxib increases miR-222 while deterring aromatase-expressing breast tumor growth in mice
title_full	Celecoxib increases miR-222 while deterring aromatase-expressing breast tumor growth in mice
title_fullStr	Celecoxib increases miR-222 while deterring aromatase-expressing breast tumor growth in mice
title_full_unstemmed	Celecoxib increases miR-222 while deterring aromatase-expressing breast tumor growth in mice
title_sort	celecoxib increases mir-222 while deterring aromatase-expressing breast tumor growth in mice
publishDate	2020
url	https://scholarbank.nus.edu.sg/handle/10635/181498
_version_	1781792528781017088

Celecoxib increases miR-222 while deterring aromatase-expressing breast tumor growth in mice

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