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* [[Lung adenocarcinoma]] (LAC): The levels of MIR22HG RNA were lower in LAC tumors than normal lung tissues and lower levels of this lncRNA in LAC tumor tissue were associated with poor patient survival times.<ref name="pmid33267888"/><ref name="pmid27338053">{{cite journal | vauthors = Li DS, Ainiwaer JL, Sheyhiding I, Zhang Z, Zhang LW | title = Identification of key long non-coding RNAs as competing endogenous RNAs for miRNA-mRNA in lung adenocarcinoma | journal = European Review for Medical and Pharmacological Sciences | volume = 20 | issue = 11 | pages = 2285–95 | date = June 2016 | pmid = 27338053 | doi = | url = }}</ref><ref name="pmid29669758">{{cite journal | vauthors = Su W, Feng S, Chen X, Yang X, Mao R, Guo C, Wang Z, Thomas DG, Lin J, Reddy RM, Orringer MB, Chang AC, Yang Z, Beer DG, Chen G | title = Silencing of Long Noncoding RNA MIR22HG Triggers Cell Survival/Death Signaling via Oncogenes YBX1, MET, and p21 in Lung Cancer | journal = Cancer Research | volume = 78 | issue = 12 | pages = 3207–3219 | date = June 2018 | pmid = 29669758 | pmc = 6004254 | doi = 10.1158/0008-5472.CAN-18-0222 | url = }}</ref>
* [[Lung adenocarcinoma]] (LAC): The levels of MIR22HG RNA were lower in LAC tumors than normal lung tissues and lower levels of this lncRNA in LAC tumor tissue were associated with poor patient survival times.<ref name="pmid33267888"/><ref name="pmid27338053">{{cite journal | vauthors = Li DS, Ainiwaer JL, Sheyhiding I, Zhang Z, Zhang LW | title = Identification of key long non-coding RNAs as competing endogenous RNAs for miRNA-mRNA in lung adenocarcinoma | journal = European Review for Medical and Pharmacological Sciences | volume = 20 | issue = 11 | pages = 2285–95 | date = June 2016 | pmid = 27338053 | doi = | url = }}</ref><ref name="pmid29669758">{{cite journal | vauthors = Su W, Feng S, Chen X, Yang X, Mao R, Guo C, Wang Z, Thomas DG, Lin J, Reddy RM, Orringer MB, Chang AC, Yang Z, Beer DG, Chen G | title = Silencing of Long Noncoding RNA MIR22HG Triggers Cell Survival/Death Signaling via Oncogenes YBX1, MET, and p21 in Lung Cancer | journal = Cancer Research | volume = 78 | issue = 12 | pages = 3207–3219 | date = June 2018 | pmid = 29669758 | pmc = 6004254 | doi = 10.1158/0008-5472.CAN-18-0222 | url = }}</ref>
* [[Non-small cell lung cancer]] (NSCLC): Low levels of MIR22HG lncRNA in NSCLC tissues were highly associated with poor patient survival times. Increasing MIR22HG lncRNA levels in cultured NSCLC cells reduced their proliferation and invasiveness. Further NSCLC cell culture studies suggested that high levels of MIR22HG lncRNA acted by suppressing the levels of [[p21]].<ref name="pmid33267888"/><ref name="pmid29669758"/>
* [[Non-small cell lung cancer]] (NSCLC): Low levels of MIR22HG lncRNA in NSCLC tissues were highly associated with poor patient survival times. Increasing MIR22HG lncRNA levels in cultured NSCLC cells reduced their proliferation and invasiveness. Further NSCLC cell culture studies suggested that high levels of MIR22HG lncRNA acted by suppressing the levels of [[p21]].<ref name="pmid33267888"/><ref name="pmid29669758"/>
*[[Hepatocellular carcinoma]] (HCC): low levels of ''MIR22HG'' lncRNA in HCC tumors were associated with short overall survival and poor disease-free survival times. The suppression of lncRNA production suppressed the growth, migration and invasion of cultured HCC cells, Further culture cell studies suggested this effect was due to the increases in [[NCOR2]] levels that were associated with decreased lncRNA levels.<ref name="pmid33267888"/>
*[[Hepatocellular carcinoma]] (HCC): low levels of ''MIR22HG'' lncRNA in HCC tumors were associated with short overall survival and poor disease-free survival times. The suppression of lncRNA production suppressed the growth, migration and invasion of cultured HCC cells, Further culture cell studies suggested this effect was due to the increases in [[NCOR2]] levels that were associated with decreased lncRNA levels.<ref name="pmid33267888"/><ref name="pmid31819482">{{cite journal | vauthors = Gao L, Xiong DD, He RQ, Yang X, Lai ZF, Liu LM, Huang ZG, Wu HY, Yang LH, Ma J, Li SH, Lin P, Yang H, Luo DZ, Dang YW, Chen G | title = MIR22HG As A Tumor Suppressive lncRNA In HCC: A Comprehensive Analysis Integrating RT-qPCR, mRNA-Seq, And Microarrays | journal = OncoTargets and Therapy | volume = 12 | issue = | pages = 9827–9848 | date = 2019 | pmid = 31819482 | pmc = 6875507 | doi = 10.2147/OTT.S227541 | url = }}</ref>
* [[cholangiocarcinoma]] (CAA): Low levels of ''MIR22HG'' lncRNA in CCA tumors were associated with an advanced clinical stage, larger tumor size, lymph node metastasis, and poor survival times.<ref name="pmid33267888"/><ref name="pmid30856284">{{cite journal | vauthors = Hu X, Tan Z, Yang Y, Yang P | title = Long non-coding RNA MIR22HG inhibits cell proliferation and migration in cholangiocarcinoma by negatively regulating the Wnt/β-catenin signaling pathway | journal = The Journal of Gene Medicine | volume = 21 | issue = 5 | pages = e3085 | date = May 2019 | pmid = 30856284 | doi = 10.1002/jgm.3085 | url = }}</ref>
* [[cholangiocarcinoma]] (CAA): Low levels of ''MIR22HG'' lncRNA in CCA tumors were associated with an advanced clinical stage, larger tumor size, lymph node metastasis, and poor survival times.<ref name="pmid33267888"/><ref name="pmid30856284">{{cite journal | vauthors = Hu X, Tan Z, Yang Y, Yang P | title = Long non-coding RNA MIR22HG inhibits cell proliferation and migration in cholangiocarcinoma by negatively regulating the Wnt/β-catenin signaling pathway | journal = The Journal of Gene Medicine | volume = 21 | issue = 5 | pages = e3085 | date = May 2019 | pmid = 30856284 | doi = 10.1002/jgm.3085 | url = }}</ref>
* [[Colorectal cancer]] (CRC): Low levels of MIR22HG lncRNA are found CRC tissues and cells.<ref name="pmid33267888"/> Cell cultured studies suggest that low levels of MiR22HF lncRNA promote [[epithelial-mesenchymal transition]] (see<ref name="pmid34459003">{{cite journal | vauthors = Brabletz S, Schuhwerk H, Brabletz T, Stemmler MP | title = Dynamic EMT: a multi-tool for tumor progression | journal = The EMBO Journal | volume = | issue = | pages = e108647 | date = August 2021 | pmid = 34459003 | doi = 10.15252/embj.2021108647 | url = }}</ref>) and thereby CRC.<ref name="pmid33267888"/><ref name="pmid32127004">{{cite journal | vauthors = Xu J, Shao T, Song M, Xie Y, Zhou J, Yin J, Ding N, Zou H, Li Y, Zhang J | title = MIR22HG acts as a tumor suppressor via TGFβ/SMAD signaling and facilitates immunotherapy in colorectal cancer | journal = Molecular Cancer | volume = 19 | issue = 1 | pages = 51 | date = March 2020 | pmid = 32127004 | pmc = 7055097 | doi = 10.1186/s12943-020-01174-w | url = }}</ref><ref name="pmid33493419">{{cite journal | vauthors = Huang GD, Liao P, Huang YH, Wu YL, Wu Y, Chen SQ, Xiong J | title = MIR22HG Regulates the Proliferation, Epithelial-Mesenchymal Transition, and Apoptosis in Colorectal Carcinoma | journal = Cancer Biotherapy & Radiopharmaceuticals | volume = | issue = | pages = | date = January 2021 | pmid = 33493419 | doi = 10.1089/cbr.2019.3509 | url = }}</ref>
* [[Colorectal cancer]] (CRC): Low levels of MIR22HG lncRNA were found in CRC tumors compared to normal colorectal tissue. Low tumor tissue levels of this lncRNA were significantly associated with shorter patient survival times. Suppressing the levels of MIR22HG lncRNA in CRC cells increased their survival and proliferation in culture and their ability to metastasize in an animal model. Further cell culture studies suggested that low levels of MiR22HF lncRNA promote [[epithelial-mesenchymal transition#In cancer progression and metastasis|epithelial-mesenchymal transition mechanisms]] (that have oncogenic actions<ref name="pmid34459003">{{cite journal | vauthors = Brabletz S, Schuhwerk H, Brabletz T, Stemmler MP | title = Dynamic EMT: a multi-tool for tumor progression | journal = The EMBO Journal | volume = | issue = | pages = e108647 | date = August 2021 | pmid = 34459003 | doi = 10.15252/embj.2021108647 | url = }}</ref>) and thereby the aggressiveness of CRC.<ref name="pmid33267888"/><ref name="pmid32127004">{{cite journal | vauthors = Xu J, Shao T, Song M, Xie Y, Zhou J, Yin J, Ding N, Zou H, Li Y, Zhang J | title = MIR22HG acts as a tumor suppressor via TGFβ/SMAD signaling and facilitates immunotherapy in colorectal cancer | journal = Molecular Cancer | volume = 19 | issue = 1 | pages = 51 | date = March 2020 | pmid = 32127004 | pmc = 7055097 | doi = 10.1186/s12943-020-01174-w | url = }}</ref><ref name="pmid33493419">{{cite journal | vauthors = Huang GD, Liao P, Huang YH, Wu YL, Wu Y, Chen SQ, Xiong J | title = MIR22HG Regulates the Proliferation, Epithelial-Mesenchymal Transition, and Apoptosis in Colorectal Carcinoma | journal = Cancer Biotherapy & Radiopharmaceuticals | volume = | issue = | pages = | date = January 2021 | pmid = 33493419 | doi = 10.1089/cbr.2019.3509 | url = }}</ref>
* [[Gastric cancer]] (GC): Low levels of ''MIR22HG'' gene expression are associated with poor 5-year overall survival in GC patients while overexpression of MIR22HG lncRNA suppressed the proliferation, invasion and migration of cultured GC cells, effects due to MIR22HG lncRNA negatively regulating [[NOTCH2]].<ref name="pmid33267888"/><ref name="pmid30539522">{{cite journal | vauthors = Qin L, Luo JZ, Tang XL, Han CG | title = Identification of Long Noncoding RNA MIR22HG as a Novel Biomarker in Thyroid Cancer | journal = Pathology Oncology Research : POR | volume = 25 | issue = 2 | pages = 703–710 | date = April 2019 | pmid = 30539522 | doi = 10.1007/s12253-018-0521-6 | url = }}</ref>
* [[Gastric cancer]] (GC): Low levels of ''MIR22HG'' gene expression were associated with poor 5-year overall survival times in GC patients. Forced overexpression of MIR22HG lncRNA suppressed the proliferation, invasiveness, and migration of cultured GC cells. Further GC cell culture studies suggested that the suppressive effects of high MIR22HG lncRNA levels were to its indirect effects in regulating [[NOTCH2]] (NOTCH2 appears involved in various types of cancer<ref name="pmid31894255">{{cite journal | vauthors = Katoh M, Katoh M | title = Precision medicine for human cancers with Notch signaling dysregulation (Review) | journal = International Journal of Molecular Medicine | volume = 45 | issue = 2 | pages = 279–297 | date = February 2020 | pmid = 31894255 | pmc = 6984804 | doi = 10.3892/ijmm.2019.4418 | url = }}</ref>).<ref name="pmid33267888"/><ref name="pmid30539522">{{cite journal | vauthors = Qin L, Luo JZ, Tang XL, Han CG | title = Identification of Long Noncoding RNA MIR22HG as a Novel Biomarker in Thyroid Cancer | journal = Pathology Oncology Research : POR | volume = 25 | issue = 2 | pages = 703–710 | date = April 2019 | pmid = 30539522 | doi = 10.1007/s12253-018-0521-6 | url = }}</ref>
* [[Prostate cancer]] (PC): Low MIR22HG lncRNA levels were found in PC cases that had a more aggressive and poorer prognosis as judged by [[Gleason score]]s, a shorter progression-free survival time, and an early onset of disease recurrences.<ref name="pmid33552133">{{cite journal | vauthors = Pudova EA, Krasnov GS, Kobelyatskaya AA, Savvateeva MV, Fedorova MS, Pavlov VS, Nyushko KM, Kaprin AD, Alekseev BY, Trofimov DY, Sukhikh GT, Snezhkina AV, Kudryavtseva AV | title = Gene Expression Changes and Associated Pathways Involved in the Progression of Prostate Cancer Advanced Stages | journal = Frontiers in Genetics | volume = 11 | issue = | pages = 613162 | date = 2020 | pmid = 33552133 | pmc = 7859645 | doi = 10.3389/fgene.2020.613162 | url = }}</ref><ref name="pmid32233607">{{cite journal | vauthors = Shen H, Weng XD, Yang D, Wang L, Liu XH | title = Long noncoding RNA MIR22HG is down-regulated in prostate cancer | journal = Mathematical Biosciences and Engineering : MBE | volume = 17 | issue = 2 | pages = 1776–1786 | date = December 2019 | pmid = 32233607 | doi = 10.3934/mbe.2020093 | url = }}</ref>
* [[Prostate cancer]] (PC): Low MIR22HG lncRNA levels were found in PC cases that had a more aggressive and poorer prognosis as judged by [[Gleason score]]s, a shorter progression-free survival time, and an early onset of disease recurrences.<ref name="pmid33552133">{{cite journal | vauthors = Pudova EA, Krasnov GS, Kobelyatskaya AA, Savvateeva MV, Fedorova MS, Pavlov VS, Nyushko KM, Kaprin AD, Alekseev BY, Trofimov DY, Sukhikh GT, Snezhkina AV, Kudryavtseva AV | title = Gene Expression Changes and Associated Pathways Involved in the Progression of Prostate Cancer Advanced Stages | journal = Frontiers in Genetics | volume = 11 | issue = | pages = 613162 | date = 2020 | pmid = 33552133 | pmc = 7859645 | doi = 10.3389/fgene.2020.613162 | url = }}</ref><ref name="pmid32233607">{{cite journal | vauthors = Shen H, Weng XD, Yang D, Wang L, Liu XH | title = Long noncoding RNA MIR22HG is down-regulated in prostate cancer | journal = Mathematical Biosciences and Engineering : MBE | volume = 17 | issue = 2 | pages = 1776–1786 | date = December 2019 | pmid = 32233607 | doi = 10.3934/mbe.2020093 | url = }}</ref>
* [[Cervical cancer|Cancer of the cervix]] (CC): Higher tumor tissue levels of MIR22HG lncRNA were associated with better clinical prognoses in CC. Forced overexpression of this lncRNA increased [[apoptosis]] (i.e. programmed cell death) and inhibited the invasiveness of several CC cell lines in culture. The cell culture studies suggested that increased lncRNA worked by suppressing the levels of a potential oncogene,<ref name="pmid33568150">{{cite journal | vauthors = Wang J, Chen L, Qiang P | title = The role of IGF2BP2, an m6A reader gene, in human metabolic diseases and cancers | journal = Cancer Cell International | volume = 21 | issue = 1 | pages = 99 | date = February 2021 | pmid = 33568150 | pmc = 7876817 | doi = 10.1186/s12935-021-01799-x | url = }}</ref> [[IGF2BP2]].<ref name="pmid32767321">{{cite journal | vauthors = Shu J, Wang D | title = Functional characterization of the long noncoding RNA MIR22HG as a tumour suppressor in cervical cancer by targeting IGF2BP2 | journal = European Review for Medical and Pharmacological Sciences | volume = 24 | issue = 15 | pages = 7953–7962 | date = August 2020 | pmid = 32767321 | doi = 10.26355/eurrev_202008_22478 | url = }}</ref><ref name="pmid32099468">{{cite journal | vauthors = Zhang Y, Zhang X, Zhu H, Liu Y, Cao J, Li D, Ding B, Yan W, Jin H, Wang S | title = Identification of Potential Prognostic Long Non-Coding RNA Biomarkers for Predicting Recurrence in Patients with Cervical Cancer | journal = Cancer Management and Research | volume = 12 | issue = | pages = 719–730 | date = 2020 | pmid = 32099468 | pmc = 7002755 | doi = 10.2147/CMAR.S231796 | url = }}</ref>
* [[Cervical cancer|Cancer of the cervix]] (CC): Higher tumor tissue levels of MIR22HG lncRNA were associated with better clinical prognoses in CC. Forced overexpression of this lncRNA increased [[apoptosis]] (i.e. programmed cell death) and inhibited the invasiveness of several CC cell lines in culture. The cell culture studies suggested that increased lncRNA worked by suppressing the levels of a potential oncogene,<ref name="pmid33568150">{{cite journal | vauthors = Wang J, Chen L, Qiang P | title = The role of IGF2BP2, an m6A reader gene, in human metabolic diseases and cancers | journal = Cancer Cell International | volume = 21 | issue = 1 | pages = 99 | date = February 2021 | pmid = 33568150 | pmc = 7876817 | doi = 10.1186/s12935-021-01799-x | url = }}</ref> [[IGF2BP2]].<ref name="pmid32767321">{{cite journal | vauthors = Shu J, Wang D | title = Functional characterization of the long noncoding RNA MIR22HG as a tumour suppressor in cervical cancer by targeting IGF2BP2 | journal = European Review for Medical and Pharmacological Sciences | volume = 24 | issue = 15 | pages = 7953–7962 | date = August 2020 | pmid = 32767321 | doi = 10.26355/eurrev_202008_22478 | url = }}</ref><ref name="pmid32099468">{{cite journal | vauthors = Zhang Y, Zhang X, Zhu H, Liu Y, Cao J, Li D, Ding B, Yan W, Jin H, Wang S | title = Identification of Potential Prognostic Long Non-Coding RNA Biomarkers for Predicting Recurrence in Patients with Cervical Cancer | journal = Cancer Management and Research | volume = 12 | issue = | pages = 719–730 | date = 2020 | pmid = 32099468 | pmc = 7002755 | doi = 10.2147/CMAR.S231796 | url = }}</ref>

Revision as of 16:59, 7 September 2021

The MIR22HG gene, i.e. the MIR22 host gene (also termed C17orf91[1], MGC14376[2] MIRN22, hsa-mir-22, or miR-22[3]), codes for a noncoding RNA (ncRNA), i.e. a RNA molecule that is not translated into a protein but nonetheless may have important functions. MIR22HG ncRNA is greater than 200 nucleotides in length and therefore informally classified as a long non-coding RNA, i.e. lncRNA. Many lncRNAs regulate diverse processes including cellular metabolism, proliferation, movement, differentiation (i.e. change of a cell from one type to another, usually more mature, cell type), apoptosis (i.e. programmed cell death), and the expression of various genes through chromatin remodeling, genomic imprinting, modulating the actions of other RNAs, and various other ways.[4][5] The MIR22HG gene is located at band 13.3 on the short (or "p") arm of chromosome 17 and is expressed in each of the 27 human tissues tested.[6] The normal actions and functions of the MIR22HG gene are extremely complex and have not been fullly defined. When overexpressed, however, it acts as a tumor suppressor gene in many cancer types but in a few cancer types it acts as an oncogene, i.e. a tumor promotor gene: MIR22HG gene's impact on various cancers is strictly dependent on the type of cancer in which it operates.[7]

The potential roles the MIR22HG gene in cancers have generally been evaluated by: a) next-generation sequencing to quantify the levels of MIR22HG RNA in cancer samples, samples of nearby normal tissue of the same type as the cancer, and cultured cancer cells of the same type as the cancers; b) comparing MIR22HG lncRNA levels in patients with the same cancer to the severity (e.g. aggressiveness, recurrence rate, and survival rate) of their cancers; c) determining the potential mechanisms for the MIR22HG lncRNA's actions, generally by defining the effects of varying the levels of this lncRNA on various cancer-promoting or cancer-inhibiting cell signaling pathways in cultured cancer cells; and d) determining the activity of these cell signaling pathways in cancer tissues. These studies are important because they established the levels of MIR22HG lncRNA as prognosis​ indicators and suggest that this lncRNA and the implicated cancerous signaling pathways are therapeutic targets for treating these cancers.[4]

MIR22HG gene tumor-suppressiping actions

Some of the cancer types that have been associated with the MIR22HG gene and its lncRNA product acting to suppress the cancer are:

  • Non-small-cell lung cancer (NSCLC): The MIR22HG gene was down-regulated (i.e. under-expressed to give low levels of this genes lncRNA) in the NSCLC tumors of individuals who had poorer prognoses.[8]. Overexpression of the MIR22HG gene in various types of NSCLC cells in culture suppressed cell proliferation and invasion and induced cell cycle arrest (i.e. blocked cell division) apparently by indirectly stimulating the production of p21, an inhibitor of cell replication.[4]
  • Thyroid cancer (TC): low levels of MIR22HG lncRNA were found in individuals with large tumor size, lymph node metastases, advanced clinical stage, shorter disease-free survival time, and poor survival times in TC. Reducing lncRNA levels using gene knockdown methods) suppressed the growth and invasiveness of TC cells in culture. Further studies suggested that these effects reflected high activity of the Hippo signaling pathway (A oncogenic pathway in TC[9]). Increasing the levels of MIR22HR lncRNA in these cultured TC cells suppressed this pathway.[4][10]
  • Lung adenocarcinoma (LAC): The levels of MIR22HG RNA were lower in LAC tumors than normal lung tissues and lower levels of this lncRNA in LAC tumor tissue were associated with poor patient survival times.[4][11][8]
  • Non-small cell lung cancer (NSCLC): Low levels of MIR22HG lncRNA in NSCLC tissues were highly associated with poor patient survival times. Increasing MIR22HG lncRNA levels in cultured NSCLC cells reduced their proliferation and invasiveness. Further NSCLC cell culture studies suggested that high levels of MIR22HG lncRNA acted by suppressing the levels of p21.[4][8]
  • Hepatocellular carcinoma (HCC): low levels of MIR22HG lncRNA in HCC tumors were associated with short overall survival and poor disease-free survival times. The suppression of lncRNA production suppressed the growth, migration and invasion of cultured HCC cells, Further culture cell studies suggested this effect was due to the increases in NCOR2 levels that were associated with decreased lncRNA levels.[4][12]
  • cholangiocarcinoma (CAA): Low levels of MIR22HG lncRNA in CCA tumors were associated with an advanced clinical stage, larger tumor size, lymph node metastasis, and poor survival times.[4][13]
  • Colorectal cancer (CRC): Low levels of MIR22HG lncRNA were found in CRC tumors compared to normal colorectal tissue. Low tumor tissue levels of this lncRNA were significantly associated with shorter patient survival times. Suppressing the levels of MIR22HG lncRNA in CRC cells increased their survival and proliferation in culture and their ability to metastasize in an animal model. Further cell culture studies suggested that low levels of MiR22HF lncRNA promote epithelial-mesenchymal transition mechanisms (that have oncogenic actions[14]) and thereby the aggressiveness of CRC.[4][15][16]
  • Gastric cancer (GC): Low levels of MIR22HG gene expression were associated with poor 5-year overall survival times in GC patients. Forced overexpression of MIR22HG lncRNA suppressed the proliferation, invasiveness, and migration of cultured GC cells. Further GC cell culture studies suggested that the suppressive effects of high MIR22HG lncRNA levels were to its indirect effects in regulating NOTCH2 (NOTCH2 appears involved in various types of cancer[17]).[4][10]
  • Prostate cancer (PC): Low MIR22HG lncRNA levels were found in PC cases that had a more aggressive and poorer prognosis as judged by Gleason scores, a shorter progression-free survival time, and an early onset of disease recurrences.[18][19]
  • Cancer of the cervix (CC): Higher tumor tissue levels of MIR22HG lncRNA were associated with better clinical prognoses in CC. Forced overexpression of this lncRNA increased apoptosis (i.e. programmed cell death) and inhibited the invasiveness of several CC cell lines in culture. The cell culture studies suggested that increased lncRNA worked by suppressing the levels of a potential oncogene,[20] IGF2BP2.[21][22]

Some reports have suggested that the MIR22HG gene acts as a tumor suppressor based on examining the effects of MIR22HG lncRNA levels on cultured cancer cell function and/or and tumor spread in animal models and/or the levels of MIR22HR lncRNA in cancer versus normal nearby tissues. However, these reports did not determine the relationship of MIR22HG levels in patients' cancer tissues to their prognoses. These reports include those on: osteosarcoma,[23] cancer of the uterus endometrium,[24] and cancer of the larynx.[25]

MIR22HG gene tumor-promoting actions

  • Glioblastoma multiforme (GBM): Increased levels of MIR22HG lncRNA were associated with poor survival in GBM patients.[4] Blocking (by Gene knockdown methods) production of this lncRNA inhibited the proliferation and invasiveness of GBM cells in culture and the growth and invasiveness of these cells in a mouse mode.[26] Further cell culture studies suggested that MIR22HG lncRNA promoted the malignancy of GBM by stimulating the Wnt/β-catenin signalling pathways.[4][26]
  • Ovarian cancer (OC): Increased levels of MIR22HG lncRNA (termed C17orf91 lncRNA in published studies) were associated with shorter progression-free survival times and tended to be associated with shorter survival times in patients with OC. Suppressing the expression of MIR22HG lncRNA by using shRNA impaired the migration, invasiveness, and viability of cultured OC cells. Elevated levels of MIR22HG lncRNA were associated with increased levels of the proto-oncogene (i.e. potentially cancer-causing gene) MYC in these culture studies.[2][4]

The MIR22HG gene acted as a tumor promotor in squamous cell carcinoma of the esophagus based on studies showing that suppressing its levels in various types of cultured esophagus squamous-cell carcinoma cells inhibited their proliferation, invasiveness, and ability to form colonies and also increased their apoptosis. The cell culture studies suggested that decreasing MIR22HG lncRNA levels produced these results by decreasing the expression of STAT3, c-Myc, and PTK2.[4]​[27]

References

  1. ^ https://www.ncbi.nlm.nih.gov/gene/84981
  2. ^ a b Li J, Yu H, Xi M, Lu X (August 2016). "Long noncoding RNA C17orf91 is a potential prognostic marker and functions as an oncogene in ovarian cancer". Journal of Ovarian Research. 9 (1): 49. doi:10.1186/s13048-016-0258-3. PMC 4989523. PMID 27535740.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  3. ^ https://www.ncbi.nlm.nih.gov/gene/?term=Homo+sapiens+MIR22
  4. ^ a b c d e f g h i j k l m n Zhang L, Li C, Su X (December 2020). "Emerging impact of the long noncoding RNA MIR22HG on proliferation and apoptosis in multiple human cancers". Journal of Experimental & Clinical Cancer Research : CR. 39 (1): 271. doi:10.1186/s13046-020-01784-8. PMC 7712612. PMID 33267888.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  5. ^ Palazzo AF, Lee ES (2015). "Non-coding RNA: what is functional and what is junk?". Frontiers in Genetics. 6: 2. doi:10.3389/fgene.2015.00002. PMC 4306305. PMID 25674102.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  6. ^ https://www.ncbi.nlm.nih.gov/gene/84981
  7. ^ Samimi H, Sajjadi-Jazi SM, Seifirad S, Atlasi R, Mahmoodzadeh H, Faghihi MA, Haghpanah V (2020). "Molecular mechanisms of long non-coding RNAs in anaplastic thyroid cancer: a systematic review". Cancer Cell International. 20: 352. doi:10.1186/s12935-020-01439-w. PMC 7392660. PMID 32760219.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  8. ^ a b c Su W, Feng S, Chen X, Yang X, Mao R, Guo C, Wang Z, Thomas DG, Lin J, Reddy RM, Orringer MB, Chang AC, Yang Z, Beer DG, Chen G (June 2018). "Silencing of Long Noncoding RNA MIR22HG Triggers Cell Survival/Death Signaling via Oncogenes YBX1, MET, and p21 in Lung Cancer". Cancer Research. 78 (12): 3207–3219. doi:10.1158/0008-5472.CAN-18-0222. PMC 6004254. PMID 29669758.
  9. ^ Carneiro T, Bim LV, Buzatto VC, Galdeno V, Asprino PF, Lee EA, Galante P, Cerutti JM (May 2021). "Evidence of Cooperation between Hippo Pathway and RAS Mutation in Thyroid Carcinomas". Cancers. 13 (10). doi:10.3390/cancers13102306. PMC 8151534. PMID 34065786. {{cite journal}}: Vancouver style error: initials in name 1 (help)CS1 maint: unflagged free DOI (link)
  10. ^ a b Qin L, Luo JZ, Tang XL, Han CG (April 2019). "Identification of Long Noncoding RNA MIR22HG as a Novel Biomarker in Thyroid Cancer". Pathology Oncology Research : POR. 25 (2): 703–710. doi:10.1007/s12253-018-0521-6. PMID 30539522.
  11. ^ Li DS, Ainiwaer JL, Sheyhiding I, Zhang Z, Zhang LW (June 2016). "Identification of key long non-coding RNAs as competing endogenous RNAs for miRNA-mRNA in lung adenocarcinoma". European Review for Medical and Pharmacological Sciences. 20 (11): 2285–95. PMID 27338053.
  12. ^ Gao L, Xiong DD, He RQ, Yang X, Lai ZF, Liu LM, Huang ZG, Wu HY, Yang LH, Ma J, Li SH, Lin P, Yang H, Luo DZ, Dang YW, Chen G (2019). "MIR22HG As A Tumor Suppressive lncRNA In HCC: A Comprehensive Analysis Integrating RT-qPCR, mRNA-Seq, And Microarrays". OncoTargets and Therapy. 12: 9827–9848. doi:10.2147/OTT.S227541. PMC 6875507. PMID 31819482.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  13. ^ Hu X, Tan Z, Yang Y, Yang P (May 2019). "Long non-coding RNA MIR22HG inhibits cell proliferation and migration in cholangiocarcinoma by negatively regulating the Wnt/β-catenin signaling pathway". The Journal of Gene Medicine. 21 (5): e3085. doi:10.1002/jgm.3085. PMID 30856284.
  14. ^ Brabletz S, Schuhwerk H, Brabletz T, Stemmler MP (August 2021). "Dynamic EMT: a multi-tool for tumor progression". The EMBO Journal: e108647. doi:10.15252/embj.2021108647. PMID 34459003.
  15. ^ Xu J, Shao T, Song M, Xie Y, Zhou J, Yin J, Ding N, Zou H, Li Y, Zhang J (March 2020). "MIR22HG acts as a tumor suppressor via TGFβ/SMAD signaling and facilitates immunotherapy in colorectal cancer". Molecular Cancer. 19 (1): 51. doi:10.1186/s12943-020-01174-w. PMC 7055097. PMID 32127004.{{cite journal}}: CS1 maint: unflagged free DOI (link)
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