Noncoding RNAs involved in the STAT3 pathway in glioma
Open accessAbstract
Glioma is the most common malignant primary brain tumour in adults. Despite improvements in neurosurgery and radiotherapy, the prognosis of glioma patients remains poor. One of the main limitations is that there are no proper clinical therapeutic targets for glioma. Therefore, it is crucial to find one or more effective targets. Signal transducer and activator of transcription 3 (STAT3) is a member of the STAT family of genes. Abnormal expression of STAT3 is involved in the process of cell proliferation, migration, invasion, immunosuppression, angiogenesis, dryness maintenance, and resistance to radiotherapy and chemotherapy in glioma. Therefore, STAT3 has been considered an ideal therapeutic target in glioma. Noncoding RNAs (ncRNAs) are a group of genes with limited or no protein-coding capacity that can regulate gene expression at the epigenetic, transcriptional and posttranscriptional level. In this review, we summarized the ncRNAs that are correlated with the ectopic expression of STAT3 in glioma.
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
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?
STAT3 binds to miR-21 promoter and regulates its expression.
“STAT3 binds to miR-21 promoter and regulates its expression.”
From miR-21 as a diagnostic and prognostic biomarker in glioma: tissue and serum expression analysis in a Pakistani cohort (2026) · cites this paper as [45]
miR-21 also regulates STAT3 gene activation and expression of hTERT in a STAT3-dependent manner.
“miR-21 also regulates STAT3 gene activation and expression of hTERT in a STAT3dependent manner [45].”
From miR-21 as a diagnostic and prognostic biomarker in glioma: tissue and serum expression analysis in a Pakistani cohort (2026) · cites this paper as [45]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Gene silencing by microRNAs: contributions of translational repression and mRNA decay
Huntzinger, E., & Izaurralde, E. (2011) · Nature Reviews Genetics · doi:10.1038/nrg2936 · Cited by 2,339 · see citing works
RNA circularization strategies in vivo and in vitro
Petkovic, S., & Müller, S. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv045 · Cited by 386 · see citing works
Flagged first, then by citations
Research works printed but not linked: 107
- [1]Allemani C Matsuda T Di Carlo V Harewood R Matz M Niksic M Bonaventure A Valkov M Johnson CJ Esteve J Global surveillance of trends in cancer survival 2000–14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries Lancet 2018 391 10125 1023 1075 10.1016/S0140-6736(17)33326-3 29395269 PMC5879496 · DOI · Paper page
- [2]Lowder L Hauenstein J Woods A Chen HR Rupji M Kowalski J Olson JJ Saxe D Schniederjan M Neill S Gliosarcoma: distinct molecular pathways and genomic alterations identified by DNA copy number/SNP microarray analysis J Neurooncol 2019 143 3 381 392 10.1007/s11060-019-03184-1 31073965 PMC6591191 · DOI
- [3]Hombach S Kretz M Non-coding RNAs: Classification, Biology and Functioning Adv Exp Med Biol 2016 937 3 17 10.1007/978-3-319-42059-2_1 27573892 · DOI
- [4]Kapranov P St Laurent G Raz T Ozsolak F Reynolds CP Sorensen PH Reaman G Milos P Arceci RJ Thompson JF The majority of total nuclear-encoded non-ribosomal RNA in a human cell is 'dark matter' un-annotated RNA BMC Biol 2010 8 149 10.1186/1741-7007-8-149 21176148 PMC3022773 · DOI
- [5]Panni S Lovering RC Porras P Orchard S Non-coding RNA regulatory networks Biochim Biophys Acta Gene Regul Mech 2020 1863 6 194417 10.1016/j.bbagrm.2019.194417 31493559 · DOI · Paper page
- [6]Chan JJ Tay Y Noncoding RNA:RNA Regulatory Networks in Cancer Int J Mol Sci 2018 19 5 PMC5983611 29702599
- [7]Song J Kim YK Targeting non-coding RNAs for the treatment of retinal diseases Mol Ther Nucleic Acids 2021 24 284 293 10.1016/j.omtn.2021.02.031 33815941 PMC7985465 · DOI
- [8]Ji W Jiao J Cheng C Shao J MicroRNA-21 in the pathogenesis of traumatic brain injury Neurochem Res 2018 43 10 1863 1868 10.1007/s11064-018-2602-z 30066160 · DOI
- [9]Ouedraogo ZG Biau J Kemeny JL Morel L Verrelle P Chautard E Role of STAT3 in genesis and progression of human malignant gliomas Mol Neurobiol 2017 54 8 5780 5797 10.1007/s12035-016-0103-0 27660268 · DOI
- [10]Lo HW Cao X Zhu H Ali-Osman F Constitutively activated STAT3 frequently coexpresses with epidermal growth factor receptor in high-grade gliomas and targeting STAT3 sensitizes them to Iressa and alkylators Clin Cancer Res 2008 14 19 6042 6054 10.1158/1078-0432.CCR-07-4923 18829483 PMC2707832 · DOI
- [11]Buettner R Mora LB Jove R Activated STAT signaling in human tumors provides novel molecular targets for therapeutic intervention Clin Cancer Res 2002 8 4 945 954 11948098
- [12]Swiatek-Machado K Kaminska B STAT signaling in glioma cells Adv Exp Med Biol 2013 986 189 208 10.1007/978-94-007-4719-7_10 22879070 · DOI
- [13]Lindemann C, Hackmann O, Delic S, Schmidt N, Reifenberger G, Riemenschneider MJAn: SOCS3 promoter methylation is mutually exclusive to EGFR amplification in gliomas and promotes glioma cell invasion through STAT3 and FAK activation. 2011, 122(2):241–251. 21590492
- [14]Brantley EC Nabors LB Gillespie GY Choi YH Palmer CA Harrison K Roarty K Benveniste EN Loss of protein inhibitors of activated STAT-3 expression in glioblastoma multiforme tumors: implications for STAT-3 activation and gene expression Clin Cancer Res 2008 14 15 4694 4704 10.1158/1078-0432.CCR-08-0618 18676737 PMC3886729 · DOI
- [15]Shi Y Guryanova OA Zhou W Liu C Huang Z Fang X Wang X Chen C Wu Q He Z Ibrutinib inactivates BMX-STAT3 in glioma stem cells to impair malignant growth and radioresistance Sci Transl Med 2018 10 443 10.1126/scitranslmed.aah6816 PMC6431250 29848664 · DOI
- [16]Sun X Wang J Huang M Chen T Chen J Zhang F Zeng H Xu Z Ke Y STAT3 promotes tumour progression in glioma by inducing FOXP1 transcription J Cell Mol Med 2018 22 11 5629 5638 10.1111/jcmm.13837 30134017 PMC6201216 · DOI
- [17]Zhang L Li Y Liu Y Wang X Chen M Xing Y Zhu D STAT3-mediated MMP-2 expression is required for 15-HETE-induced vascular adventitial fibroblast migration J Steroid Biochem Mol Biol 2015 149 106 117 10.1016/j.jsbmb.2015.01.015 25623089 · DOI
- [18]Kang SH Yu MO Park KJ Chi SG Park DH Chung YG Activated STAT3 regulates hypoxia-induced angiogenesis and cell migration in human glioblastoma Neurosurgery 2010 67 5 1386 1395 10.1227/NEU.0b013e3181f1c0cd 20871442 · DOI
- [19]Yang XO Panopoulos AD Nurieva R Chang SH Wang D Watowich SS Dong C STAT3 regulates cytokine-mediated generation of inflammatory helper T cells J Biol Chem 2007 282 13 9358 9363 10.1074/jbc.C600321200 17277312 · DOI
- [20]Zhang M Zhou L Xu Y Yang M Xu Y Komaniecki GP Kosciuk T Chen X Lu X Zou X A STAT3 palmitoylation cycle promotes TH17 differentiation and colitis Nature 2020 586 7829 434 439 10.1038/s41586-020-2799-2 33029007 PMC7874492 · DOI
- [21]Yuan X Du J Hua S Zhang H Gu C Wang J Yang L Huang J Yu J Liu F Suppression of autophagy augments the radiosensitizing effects of STAT3 inhibition on human glioma cells Exp Cell Res 2015 330 2 267 276 10.1016/j.yexcr.2014.09.006 25220423 · DOI
- [22]Tan MSY Sandanaraj E Chong YK Lim SW Koh LWH Ng WH Tan NS Tan P Ang BT Tang C A STAT3-based gene signature stratifies glioma patients for targeted therapy Nat Commun 2019 10 1 3601 10.1038/s41467-019-11614-x 31399589 PMC6689009 · DOI
- [23]Abreu FB Liu X Tsongalis GJ miRNA analysis in pancreatic cancer: the Dartmouth experience Clin Chem Lab Med 2017 55 5 755 762 10.1515/cclm-2017-0046 28343174 · DOI
- [24]Lee Y Kim M Han J Yeom KH Lee S Baek SH Kim VN MicroRNA genes are transcribed by RNA polymerase II EMBO J 2004 23 20 4051 4060 10.1038/sj.emboj.7600385 15372072 PMC524334 · DOI
- [25]Lee Y Ahn C Han J Choi H Kim J Yim J Lee J Provost P Radmark O Kim S The nuclear RNase III Drosha initiates microRNA processing Nature 2003 425 6956 415 419 10.1038/nature01957 14508493 · DOI
- [26]Wang J Lee JE Riemondy K Yu Y Marquez SM Lai EC Yi R XPO5 promotes primary miRNA processing independently of RanGTP Nat Commun 2020 11 1 1845 10.1038/s41467-020-15598-x 32296071 PMC7160132 · DOI
- [27]Saliminejad K Khorram Khorshid HR Soleymani Fard S Ghaffari SH An overview of microRNAs: Biology, functions, therapeutics, and analysis methods J Cell Physiol 2019 234 5 5451 5465 10.1002/jcp.27486 30471116 · DOI
- [28]Achkar NP Cambiagno DA Manavella PA miRNA Biogenesis: A Dynamic Pathway Trends Plant Sci 2016 21 12 1034 1044 10.1016/j.tplants.2016.09.003 27793495 · DOI
- [29]Olejniczak M Kotowska-Zimmer A Krzyzosiak W Stress-induced changes in miRNA biogenesis and functioning Cell Mol Life Sci 2018 75 2 177 191 10.1007/s00018-017-2591-0 28717872 PMC5756259 · DOI
- [30]Kabekkodu SP Shukla V Varghese VK D'Souza J Chakrabarty S Satyamoorthy K Clustered miRNAs and their role in biological functions and diseases Biol Rev 2018 93 4 1955 86 10.1111/brv.12428 29797774 · DOI
- [31]Fabian MR Sonenberg N Filipowicz W Regulation of mRNA translation and stability by microRNAs Annu Rev Biochem 2010 79 351 379 10.1146/annurev-biochem-060308-103103 20533884 · DOI · Paper page
- [33]Rouleau S Glouzon JS Brumwell A Bisaillon M Perreault JP 3' UTR G-quadruplexes regulate miRNA binding RNA 2017 23 8 1172 1179 10.1261/rna.060962.117 28473452 PMC5513062 · DOI
- [34]Xu H Zhao G Zhang Y Jiang H Wang W Zhao D Hong J Yu H Qi L Mesenchymal stem cell-derived exosomal microRNA-133b suppresses glioma progression via Wnt/beta-catenin signaling pathway by targeting EZH2 Stem Cell Res Ther 2019 10 1 381 10.1186/s13287-019-1446-z 31842978 PMC6915914 · DOI
- [35]Wang S Yin Y Liu S Roles of microRNAs during glioma tumorigenesis and progression Histol Histopathol 2019 34 3 213 222 30215456
- [36]Ye X Wei W Zhang Z He C Yang R Zhang J Wu Z Huang Q Jiang Q Identification of microRNAs associated with glioma diagnosis and prognosis Oncotarget 2017 8 16 26394 26403 10.18632/oncotarget.14445 28060761 PMC5432266 · DOI
- [37]Ji W Jiao J Cheng C Xiao Y Shao J Liu H A positive feedback loop of LINC00662 and STAT3 promotes malignant phenotype of glioma Pathol Res Pract 2021 224 153539 10.1016/j.prp.2021.153539 34246852 · DOI
- [38]Siddiqui WA Ahad A Ahsan H The mystery of BCL2 family: Bcl-2 proteins and apoptosis: an update Arch Toxicol 2015 89 3 289 317 10.1007/s00204-014-1448-7 25618543 · DOI
- [39]Doherty J Baehrecke EH Life, death and autophagy Nat Cell Biol 2018 20 10 1110 1117 10.1038/s41556-018-0201-5 30224761 PMC9721133 · DOI
- [40]Yang ZY Wang Y Liu Q Wu M microRNA cluster MC-let-7a-1~let-7d promotes autophagy and apoptosis of glioma cells by down-regulating STAT3 CNS Neurosci Ther 2020 26 3 319 331 10.1111/cns.13273 31868319 PMC7052808 · DOI
- [41]Yu-Ju WuC Chen CH Lin CY Feng LY Lin YC Wei KC Huang CY Fang JY Chen PY CCL5 of glioma-associated microglia/macrophages regulates glioma migration and invasion via calcium-dependent matrix metalloproteinase 2 Neuro Oncol 2020 22 2 253 266 10.1093/neuonc/noz189 31593589 PMC7032635 · DOI
- [42]Peng T Zhou L Zuo L Luan Y MiR-506 functions as a tumor suppressor in glioma by targeting STAT3 Oncol Rep 2016 35 2 1057 1064 10.3892/or.2015.4406 26554866 · DOI
- [43]Liu HW Lee PM Bamodu OA Su YK Fong IH Yeh CT Chien MH Kan IH Lin CM Enhanced Hsa-miR-181d/p-STAT3 and Hsa-miR-181d/p-STAT5A Ratios Mediate the Anticancer Effect of Garcinol in STAT3/5A-Addicted Glioblastoma Cancers (Basel) 2019 11 12 PMC6966688 31783691
- [44]Choi S Yu Y Grimmer MR Wahl M Chang SM Costello JF Temozolomide-associated hypermutation in gliomas Neuro Oncol 2018 20 10 1300 1309 10.1093/neuonc/noy016 29452419 PMC6120358 · DOI
- [45]Xu JX Yang Y Zhang X Luan XP MicroRNA-29b promotes cell sensitivity to Temozolomide by targeting STAT3 in glioma Eur Rev Med Pharmacol Sci 2020 24 4 1922 1931 32141561
- [46]Hong L Ya-Wei L Hai W Qiang Z Jun-Jie L Huang A Song-Tao Q Yun-Tao L MiR-519a functions as a tumor suppressor in glioma by targeting the oncogenic STAT3 pathway J Neurooncol 2016 128 1 35 45 10.1007/s11060-016-2095-z 26970980 · DOI
- [47]Li H Chen L Li JJ Zhou Q Huang A Liu WW Wang K Gao L Qi ST Lu YT miR-519a enhances chemosensitivity and promotes autophagy in glioblastoma by targeting STAT3/Bcl2 signaling pathway J Hematol Oncol 2018 11 1 70 10.1186/s13045-018-0618-0 29843746 PMC5975545 · DOI
- [48]Wei J Wang F Kong LY Xu S Doucette T Ferguson SD Yang Y McEnery K Jethwa K Gjyshi O miR-124 inhibits STAT3 signaling to enhance T cell-mediated immune clearance of glioma Cancer Res 2013 73 13 3913 3926 10.1158/0008-5472.CAN-12-4318 23636127 PMC3780786 · DOI
- [49]Li C Li H Zhang P Yu LJ Huang TM Song X Kong QY Dong JL Li PN Liu J SHP2, SOCS3 and PIAS3 Expression Patterns in Medulloblastomas: Relevance to STAT3 Activation and Resveratrol-Suppressed STAT3 Signaling Nutrients 2016 9 1 10.3390/nu9010003 PMC5295047 28035977 · DOI
- [50]Xu CH Liu Y Xiao LM Chen LK Zheng SY Zeng EM Li DH Li YP Silencing microRNA-221/222 cluster suppresses glioblastoma angiogenesis by suppressor of cytokine signaling-3-dependent JAK/STAT pathway J Cell Physiol 2019 234 12 22272 22284 10.1002/jcp.28794 31106423 · DOI
- [51]Che S Sun T Wang J Jiao Y Wang C Meng Q Qi W Yan Z miR-30 overexpression promotes glioma stem cells by regulating Jak/STAT3 signaling pathway Tumour Biol 2015 36 9 6805 6811 10.1007/s13277-015-3400-8 25840690 · DOI
- [52]Jiao J Zhang R Li Z Yin Y Fang X Ding X Cai Y Yang S Mu H Zong D Nuclear Smad6 promotes gliomagenesis by negatively regulating PIAS3-mediated STAT3 inhibition Nat Commun 2018 9 1 2504 10.1038/s41467-018-04936-9 29950561 PMC6021382 · DOI
- [53]Shi L Wan Y Sun G Zhang S Wang Z Zeng Y miR-125b inhibitor may enhance the invasion-prevention activity of temozolomide in glioblastoma stem cells by targeting PIAS3 BioDrugs 2014 28 1 41 54 10.1007/s40259-013-0053-2 23857508 · DOI
- [54]Song ZB Yang HP Xu AQ Zhan ZM Song Y Li ZY Connective tissue growth factor as an unfavorable prognostic marker promotes the proliferation, migration, and invasion of gliomas Chin Med J (Engl) 2020 6 670 678 10.1097/CM9.0000000000000683 PMC7190229 32197031 · DOI
- [55]Zhang P Chen FZ Jia QB Hu DF Upregulation of microRNA-133a and downregulation of connective tissue growth factor suppress cell proliferation, migration, and invasion in human glioma through the JAK/STAT signaling pathway IUBMB Life 2019 71 12 1857 1875 10.1002/iub.2126 31381269 · DOI
- [56]Zhang Z Gong Q Li M Xu J Zheng Y Ge P Chi G MicroRNA-124 inhibits the proliferation of C6 glioma cells by targeting Smad4 Int J Mol Med 2017 40 4 1226 1234 10.3892/ijmm.2017.3088 28791348 · DOI
- [57]Vallath S Sage EK Kolluri KK Lourenco SN Teixeira VS Chimalapati S George PJ Janes SM Giangreco A CADM1 inhibits squamous cell carcinoma progression by reducing STAT3 activity Sci Rep 2016 6 24006 10.1038/srep24006 27035095 PMC4817512 · DOI
- [58]Cai Q Zhu A Gong L Exosomes of glioma cells deliver miR-148a to promote proliferation and metastasis of glioblastoma via targeting CADM1 Bull Cancer 2018 105 7–8 643 651 10.1016/j.bulcan.2018.05.003 29921422 · DOI
- [59]Saito K Ohta S Kawakami Y Yoshida K Toda M Functional analysis of KIF20A, a potential immunotherapeutic target for glioma J Neurooncol 2017 132 1 63 74 10.1007/s11060-016-2360-1 28070829 · DOI
- [60]Tang J Xu J Zhi Z Wang X Wang Y Zhou Y Chen R MiR-876-3p targets KIF20A to block JAK2/STAT3 pathway in glioma Am J Transl Res 2019 11 8 4957 4966 31497212 PMC6731397
- [61]Heimberger AB McGary EC Suki D Ruiz M Wang H Fuller GN Bar-Eli M Loss of the AP-2alpha transcription factor is associated with the grade of human gliomas Clin Cancer Res 2005 11 1 267 272 15671555
- [62]Huang W Zhong Z Luo C Xiao Y Li L Zhang X Yang L Xiao K Ning Y Chen L The miR-26a/AP-2alpha/Nanog signaling axis mediates stem cell self-renewal and temozolomide resistance in glioma Theranostics 2019 9 19 5497 5516 10.7150/thno.33800 31534499 PMC6735392 · DOI
- [63]Cao F Zhang Q Chen W Zheng F Ran Q He Y Gao Y Yao S miR-6743–5p, as a direct upstream regulator of GRIM-19, enhances proliferation and suppresses apoptosis in glioma cells Biosci Rep 2017 37 6 10.1042/BSR20171038 PMC5725612 29074558 · DOI
- [64]Cheng J Meng J Zhu L Peng Y Exosomal noncoding RNAs in Glioma: biological functions and potential clinical applications Mol Cancer 2020 19 1 66 10.1186/s12943-020-01189-3 32213181 PMC7098115 · DOI
- [65]Qian M Wang S Guo X Wang J Zhang Z Qiu W Gao X Chen Z Xu J Zhao R Hypoxic glioma-derived exosomes deliver microRNA-1246 to induce M2 macrophage polarization by targeting TERF2IP via the STAT3 and NF-kappaB pathways Oncogene 2020 39 2 428 442 10.1038/s41388-019-0996-y 31485019 · DOI · Paper page
- [66]Cancer Genome Atlas Research N: Comprehensive genomic characterization defines human glioblastoma genes and core pathways. Nature 2008, 455(7216): 1061–1068. PMC2671642 18772890
- [67]Huang T Alvarez AA Pangeni RP Horbinski CM Lu S Kim SH James CD Brenann CW A regulatory circuit of miR-125b/miR-20b and Wnt signalling controls glioblastoma phenotypes through FZD6-modulated pathways Nat Commun 2016 7 12885 10.1038/ncomms12885 27698350 PMC5059456 · DOI
- [68]Ohno M Natsume A Kondo Y Iwamizu H Motomura K Toda H Ito M Kato T Wakabayashi T The modulation of microRNAs by type I IFN through the activation of signal transducers and activators of transcription 3 in human glioma Mol Cancer Res 2009 7 12 2022 2030 10.1158/1541-7786.MCR-09-0319 19934272 · DOI
- [69]Ray S Coulter DW Gray SD Sughroue JA Roychoudhury S McIntyre EM Chaturvedi NK Bhakat KK Joshi SS McGuire TR Suppression of STAT3 NH2 -terminal domain chemosensitizes medulloblastoma cells by activation of protein inhibitor of activated STAT3 via de-repression by microRNA-21 Mol Carcinog 2018 57 4 536 548 10.1002/mc.22778 29280516 PMC6132241 · DOI
- [70]Han L Yue X Zhou X Lan FM You G Zhang W Zhang KL Zhang CZ Cheng JQ Yu SZ MicroRNA-21 expression is regulated by beta-catenin/STAT3 pathway and promotes glioma cell invasion by direct targeting RECK CNS Neurosci Ther 2012 18 7 573 583 10.1111/j.1755-5949.2012.00344.x 22630347 PMC6493520 · DOI
- [71]Wang YY Sun G Luo H Wang XF Lan FM Yue X Fu LS Pu PY Kang CS Liu N MiR-21 modulates hTERT through a STAT3-dependent manner on glioblastoma cell growth CNS Neurosci Ther 2012 18 9 722 728 10.1111/j.1755-5949.2012.00349.x 22709411 PMC6493453 · DOI
- [72]Xue J Zhou A Wu Y Morris SA Lin K Amin S Verhaak R Fuller G Xie K Heimberger AB miR-182-5p Induced by STAT3 Activation Promotes Glioma Tumorigenesis Cancer Res 2016 76 14 4293 4304 10.1158/0008-5472.CAN-15-3073 27246830 PMC5033679 · DOI
- [73]Yin J Ge X Shi Z Yu C Lu C Wei Y Zeng A Wang X Yan W Zhang J Extracellular vesicles derived from hypoxic glioma stem-like cells confer temozolomide resistance on glioblastoma by delivering miR-30b-3p Theranostics 2021 11 4 1763 1779 10.7150/thno.47057 33408780 PMC7778586 · DOI
- [74]Mathew LK Huangyang P Mucaj V Lee SS Skuli N Eisinger-Mathason TS Biju K Li B Venneti S Lal P Feedback circuitry between miR-218 repression and RTK activation in glioblastoma Sci Signal 2015 8 375 42 10.1126/scisignal.2005978 PMC4437515 25943352 · DOI
- [75]Wang H Feng H Zhang Y Resveratrol inhibits hypoxia-induced glioma cell migration and invasion by the p-STAT3/miR-34a axis Neoplasma 2016 63 4 532 539 10.4149/neo_2016_406 27268916 · DOI
- [76]Zhang X Ding H Han Y Sun D Wang H Zhai XU The significance of microRNA-184 on JAK2/STAT3 signaling pathway in the formation mechanism of glioblastoma Oncol Lett 2015 10 6 3510 3514 10.3892/ol.2015.3798 26788159 PMC4665810 · DOI
- [77]Chang JH Hwang YH Lee DJ Kim DH Park JM Wu HG Kim IA MicroRNA-203 Modulates the Radiation Sensitivity of Human Malignant Glioma Cells Int J Radiat Oncol Biol Phys 2016 94 2 412 420 10.1016/j.ijrobp.2015.10.001 26678661 · DOI
- [78]Zhou RJ Xu XY Liu BX Dai WZ Cai MQ Bai CF Zhang XF Wang LM Lin L Jia SZ Growth-inhibitory and chemosensitizing effects of microRNA-31 in human glioblastoma multiforme cells Int J Mol Med 2015 36 4 1159 1164 10.3892/ijmm.2015.2312 26310668 · DOI
- [79]Chen L Li H Han L Zhang K Wang G Wang Y Liu Y Zheng Y Jiang T Pu P Expression and function of miR-27b in human glioma Oncol Rep 2011 26 6 1617 1621 21922148
- [80]Yang CM Chiba T Brill B Delis N von Manstein V Vafaizadeh V Oellerich T Groner B Expression of the miR-302/367 cluster in glioblastoma cells suppresses tumorigenic gene expression patterns and abolishes transformation related phenotypes Int J Cancer 2015 137 10 2296 2309 10.1002/ijc.29606 25991553 PMC4744715 · DOI
- [81]Zheng F Wang M Li Y Huang C Tao D Xie F Zhang H Sun J Zhang C Gu C CircNR3C1 inhibits proliferation of bladder cancer cells by sponging miR-27a-3p and downregulating cyclin D1 expression Cancer Lett 2019 460 139 151 10.1016/j.canlet.2019.06.018 31255724 · DOI
- [82]Kopp F Mendell JT Functional classification and experimental dissection of long noncoding RNAs Cell 2018 172 3 393 407 10.1016/j.cell.2018.01.011 29373828 PMC5978744 · DOI
- [83]Zhu J Fu H Wu Y Zheng X Function of lncRNAs and approaches to lncRNA-protein interactions Sci China Life Sci 2013 56 10 876 885 10.1007/s11427-013-4553-6 24091684 · DOI
- [84]Engreitz JM Haines JE Perez EM Munson G Chen J Kane M McDonel PE Guttman M Lander ES Local regulation of gene expression by lncRNA promoters, transcription and splicing Nature 2016 539 7629 452 455 10.1038/nature20149 27783602 PMC6853796 · DOI · Paper page
- [85]Shi J Dong B Cao J Mao Y Guan W Peng Y Wang S Long non-coding RNA in glioma: signaling pathways Oncotarget 2017 8 16 27582 27592 10.18632/oncotarget.15175 28187439 PMC5432359 · DOI
- [86]Liu H Li C Yang J Sun Y Zhang S Yang J Yang L Wang Y Jiao B Long noncoding RNA CASC9/miR-519d/STAT3 positive feedback loop facilitate the glioma tumourigenesis J Cell Mol Med 2018 22 12 6338 6344 10.1111/jcmm.13932 30270508 PMC6237610 · DOI
- [87]Zheng J Liu X Wang P Xue Y Ma J Qu C Liu Y CRNDE promotes malignant progression of glioma by attenuating miR-384/PIWIL4/STAT3 Axis Mol Ther 2016 24 7 1199 1215 10.1038/mt.2016.71 27058823 PMC5088760 · DOI
- [88]Tang J, Yu B, Li Y, Zhang W, Alvarez AA, Hu B, Cheng SY, Feng H: TGF-beta-activated lncRNA LINC00115 is a critical regulator of glioma stem-like cell tumorigenicity. EMBO Rep 2019, 20(12):e48170. PMC6893290 31599491
- [89]Wu W Yu T Wu Y Tian W Zhang J Wang Y The miR155HG/miR-185/ANXA2 loop contributes to glioblastoma growth and progression J Exp Clin Cancer Res 2019 38 1 133 10.1186/s13046-019-1132-0 30898167 PMC6427903 · DOI
- [90]Liang J Liu N Xin H Knockdown long non-coding RNA PEG10 inhibits proliferation, migration and invasion of glioma cell line U251 by regulating miR-506 Gen Physiol Biophys 2019 38 4 295 304 10.4149/gpb_2019018 31241046 · DOI
- [91]Cao W Liu B Ma H Long non-coding RNA GHET1 promotes viability, migration and invasion of glioma cell line U251 by down-regulation of miR-216a Eur Rev Med Pharmacol Sci 2019 23 4 1591 1599 30840282
- [92]Dong N Guo J Han S Bao L Diao Y Lin Z Positive feedback loop of lncRNA HOXC-AS2/miR-876-5p/ZEB1 to regulate EMT in glioma Onco Targets Ther 2019 12 7601 7609 10.2147/OTT.S216134 31571911 PMC6754333 · DOI
- [93]Hu YW Kang CM Zhao JJ Nie Y Zheng L Li HX Li X Wang Q Qiu YR LncRNA PLAC2 down-regulates RPL36 expression and blocks cell cycle progression in glioma through a mechanism involving STAT1 J Cell Mol Med 2018 22 1 497 510 10.1111/jcmm.13338 28922548 PMC5742712 · DOI
- [95]Du WW Zhang C Yang W Yong T Awan FM Yang BB Identifying and Characterizing circRNA-Protein Interaction Theranostics 2017 7 17 4183 4191 10.7150/thno.21299 29158818 PMC5695005 · DOI
- [96]Zhou ZB Huang GX Fu Q Han B Lu JJ Chen AM Zhu L circRNA.33186 contributes to the pathogenesis of osteoarthritis by sponging miR-127–5p Mol Ther 2019 27 3 531 541 10.1016/j.ymthe.2019.01.006 30692016 PMC6402950 · DOI
- [97]Ashwal-Fluss R Meyer M Pamudurti NR Ivanov A Bartok O Hanan M Evantal N Memczak S Rajewsky N Kadener S circRNA biogenesis competes with pre-mRNA splicing Mol Cell 2014 56 1 55 66 10.1016/j.molcel.2014.08.019 25242144 · DOI · Paper page
- [98]Zheng Q Bao C Guo W Li S Chen J Chen B Luo Y Lyu D Li Y Shi G Circular RNA profiling reveals an abundant circHIPK3 that regulates cell growth by sponging multiple miRNAs Nat Commun 2016 7 11215 10.1038/ncomms11215 27050392 PMC4823868 · DOI
- [99]He Q Zhao L Liu X Zheng J Liu Y Liu L Ma J Cai H Li Z Xue Y MOV10 binding circ-DICER1 regulates the angiogenesis of glioma via miR-103a-3p/miR-382-5p mediated ZIC4 expression change J Exp Clin Cancer Res 2019 38 1 9 10.1186/s13046-018-0990-1 30621721 PMC6323715 · DOI
- [100]Lei B Huang Y Zhou Z Zhao Y Thapa AJ Li W Cai W Deng Y Circular RNA hsa_circ_0076248 promotes oncogenesis of glioma by sponging miR-181a to modulate SIRT1 expression J Cell Biochem 2019 120 4 6698 6708 10.1002/jcb.27966 30506951 PMC6587862 · DOI
- [101]Wang Y Sui X Zhao H Cong L Li Y Xin T Guo M Hao W Decreased circular RNA hsa_circ_0001649 predicts unfavorable prognosis in glioma and exerts oncogenic properties in vitro and in vivo Gene 2018 676 117 122 10.1016/j.gene.2018.07.037 30016668 · DOI
- [102]Hu D Zhang Y Circular RNA HIPK3 promotes glioma progression by binding to miR-124-3p Gene 2019 690 81 89 10.1016/j.gene.2018.11.073 30576808 · DOI
- [103]Wang J Zhang Y Song H Yin H Jiang T Xu Y Liu L Wang H Gao H Wang R The circular RNA circSPARC enhances the migration and proliferation of colorectal cancer by regulating the JAK/STAT pathway Mol Cancer 2021 20 1 81 10.1186/s12943-021-01375-x 34074294 PMC8167978 · DOI
- [104]Zhang X Yang J Bian Z Shi D Cao Z Long noncoding RNA DANCR promotes nasopharyngeal carcinoma progression by interacting with STAT3, enhancing IL-6/JAK1/STAT3 signaling Biomed Pharmacother 2019 113 108713 10.1016/j.biopha.2019.108713 30849642 · DOI
- [105]Tan Y Wang Y Zou Y Zhou C Yi Y Ling Y Liao F Jiang Y Peng X LncRNA LOC101927514 regulates PM25-driven inflammation in human bronchial epithelial cells through binding p-STAT3 protein Toxicol Lett 2020 319 119 128 10.1016/j.toxlet.2019.10.009 31682869 · DOI
- [106]Liu J Yang Q Sun H Wang X Saiyin H Zhang H The circ-AMOTL1/ENO1 axis implicated in the tumorigenesis of OLP-associated oral squamous cell carcinoma Cancer Manag Res 2020 12 7219 7230 10.2147/CMAR.S251348 32884340 PMC7440838 · DOI
- [107]Tang WG Hu B Sun HX Sun QM Sun C Fu PY Yang ZF Zhang X Zhou CH Fan J Long non-coding RNA00364 represses hepatocellular carcinoma cell proliferation via modulating p-STAT3-IFIT2 signaling axis Oncotarget 2017 8 60 102006 102019 10.18632/oncotarget.22039 29254221 PMC5731931 · DOI
- [108]Guo X Xue H Shao Q Wang J Guo X Chen X Zhang J Xu S Li T Zhang P Hypoxia promotes glioma-associated macrophage infiltration via periostin and subsequent M2 polarization by upregulating TGF-beta and M-CSFR Oncotarget 2016 7 49 80521 80542 10.18632/oncotarget.11825 27602954 PMC5348338 · DOI
- [109]Zhang Y Li X Zhang J Liang H Natural killer T cell cytotoxic activity in cervical cancer is facilitated by the LINC00240/microRNA-124-3p/STAT3/MICA axis Cancer Lett 2020 474 63 73 10.1016/j.canlet.2019.12.038 31904481 · DOI
Cited by
Sorted by citations
Laghari, A. A., Sufiyan, S., Amin, W., Ilyas, S., Naeem, S., Adnan, U., Abidi, S. H., Uddin, S., Enam, S. A., & Mughal, N. (2026) · Journal of Neuro-Oncology · doi:10.1007/s11060-025-05287-4 · Cited by 1 · see citing works
“In addition, STAT3 signaling is closely tied to miR-21: STAT3 binds the miR-21 promoter to enhance expression, while miR-21 also regulates STAT3 gene activation and expression of hTERT in a STAT3-dependent manner [45].”
- Authors
- Bian, Z., Ji, W., Xu, B., Huo, Z., Huang, H., Huang, J., Jiao, J., Shao, J., & Zhang, X.
- Affiliations
- Wuxi People's Hospital (CN)
- Corresponding author
- Shao, Junfei
- Zhang, Xiaolu
- Venue
- Cancer Cell International
- Published
- 2021-08-23
- Volume
- 21
- Issue
- 1
- Pages
- 445-445
- ISSN
- 1475-2867 (ISSN-L)
- PMC
- PMC8381529
- OpenAlex
- W3194035584
- Cited by
- 28
- References
- 2
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 6 · 2023: 9 · 2022: 6 · 2021: 1
- FWCI
- 0.66
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Cancer Cell International (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Innovative Research Group Project of the National Natural Science Foundation of China (81672487)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
- Health Sciences › Medicine › Genetics › Glioma Diagnosis and Treatment
- Health Sciences › Medicine › Oncology › Cytokine Signaling Pathways and Interactions
- Keywords
- glioma, STAT3 signaling, non-coding RNA, therapeutic target, epigenetic regulation, post-transcriptional regulation, radiotherapy resistance, chemoresistance, tumor immunosuppression, tumor angiogenesis, cell proliferation and invasion
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