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    MEST mesoderm specific transcript [ Homo sapiens (human) ]

    Gene ID: 4232, updated on 2-May-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    alpha1,3-fucosylation of MEST promotes invasion potential of cytotrophoblast cells by activating translation initiation.

    α1,3-fucosylation of MEST promotes invasion potential of cytotrophoblast cells by activating translation initiation.
    Wang H, Cui X, Wang L, Fan N, Yu M, Qin H, Liu S, Yan Q., Free PMC Article

    11/1/2023
    Genome-wide CRISPR/Cas9 screening identifies a targetable MEST-PURA interaction in cancer metastasis.

    Genome-wide CRISPR/Cas9 screening identifies a targetable MEST-PURA interaction in cancer metastasis.
    Xu WW, Liao L, Dai W, Zheng CC, Tan XP, He Y, Zhang QH, Huang ZH, Chen WY, Qin YR, Chen KS, He ML, Law S, Lung ML, He QY, Li B., Free PMC Article

    06/21/2023
    MiR-29c-3p represses gastric cancer development via modulating MEST.

    MiR-29c-3p represses gastric cancer development via modulating MEST.
    Li H, Lv J, Wang J, Wang H, Luo L.

    05/4/2023
    Human umbilical cord blood mesenchymal stem cells-derived exosomal microRNA-503-3p inhibits progression of human endometrial cancer cells through downregulating MEST.

    Human umbilical cord blood mesenchymal stem cells-derived exosomal microRNA-503-3p inhibits progression of human endometrial cancer cells through downregulating MEST.
    Pan Y, Wang X, Li Y, Yan P, Zhang H.

    08/27/2022
    Increased co-expression of MEST and BRCA1 is associated with worse prognosis and immune infiltration in ovarian cancer.

    Increased co-expression of MEST and BRCA1 is associated with worse prognosis and immune infiltration in ovarian cancer.
    Zhang J, Yu S, Li Q, Wang Q, Zhang J.

    04/30/2022
    miR-145-5p Modulates Gefitinib Resistance by Targeting NRAS and MEST in Non-Small Cell Lung Cancer.

    miR-145-5p Modulates Gefitinib Resistance by Targeting NRAS and MEST in Non-Small Cell Lung Cancer.
    Yu C, Li B, Wang J, Zhang Z, Li S, Lei S, Wang Q.

    02/12/2022
    MEST promotes lung cancer invasion and metastasis by interacting with VCP to activate NF-kappaB signaling.

    MEST promotes lung cancer invasion and metastasis by interacting with VCP to activate NF-κB signaling.
    Wang Y, Zhang J, Li YJ, Yu NN, Liu WT, Liang JZ, Xu WW, Sun ZH, Li B, He QY., Free PMC Article

    02/5/2022
    Hypermethylation of Mest promoter causes aberrant Wnt signaling in patients with Alzheimer's disease.

    Hypermethylation of Mest promoter causes aberrant Wnt signaling in patients with Alzheimer's disease.
    Prasad R, Jung H, Tan A, Song Y, Moon S, Shaker MR, Sun W, Lee J, Ryu H, Lim HK, Jho EH., Free PMC Article

    01/29/2022
    The effect of folic acid deficiency on Mest/Peg1 in neural tube defects.

    The effect of folic acid deficiency on Mest/Peg1 in neural tube defects.
    Chang S, Jing J, Shangguan S, Li B, Yao X, Liu X, Zhang T, Wu J, Wang L.

    11/13/2021
    The sperm epigenome does not display recurrent epimutations in patients with severely impaired spermatogenesis.

    The sperm epigenome does not display recurrent epimutations in patients with severely impaired spermatogenesis.
    Leitão E, Di Persio S, Laurentino S, Wöste M, Dugas M, Kliesch S, Neuhaus N, Horsthemke B., Free PMC Article

    06/5/2021
    MEST induces Twist-1-mediated EMT through STAT3 activation in breast cancers.

    MEST induces Twist-1-mediated EMT through STAT3 activation in breast cancers.
    Kim MS, Lee HS, Kim YJ, Lee DY, Kang SG, Jin W., Free PMC Article

    10/3/2020
    Long intergenic noncoding RNA (LINC00) 284 (LINC00284) is involved in angiogenesis during ovarian cancer (OC) development by recruiting nuclear factor kappa B (NF-kappaB1) and down-regulating mesoderm-specific transcript (MEST).

    Long intergenic noncoding RNA LINC00284 knockdown reduces angiogenesis in ovarian cancer cells via up-regulation of MEST through NF-κB1.
    Ruan Z, Zhao D., Free PMC Article

    06/13/2020
    Imprinting methylation in SNRPN and MEST1 in adult blood predicts cognitive ability.

    Imprinting methylation in SNRPN and MEST1 in adult blood predicts cognitive ability.
    Lorgen-Ritchie M, Murray AD, Ferguson-Smith AC, Richards M, Horgan GW, Phillips LH, Hoad G, Gall I, Harrison K, McNeill G, Ito M, Haggarty P., Free PMC Article

    11/9/2019
    Study provides evidence that MEST mediates the impact of prenatal bisphenol A exposure on long-term body weight development in offspring by triggering adipocyte differentiation.

    MEST mediates the impact of prenatal bisphenol A exposure on long-term body weight development.
    Junge KM, Leppert B, Jahreis S, Wissenbach DK, Feltens R, Grützmann K, Thürmann L, Bauer T, Ishaque N, Schick M, Bewerunge-Hudler M, Röder S, Bauer M, Schulz A, Borte M, Landgraf K, Körner A, Kiess W, von Bergen M, Stangl GI, Trump S, Eils R, Polte T, Lehmann I., Free PMC Article

    05/25/2019
    We conclude methylation changes at some CpG sites of MEST and DLK differentially methylated regions in preeclamptic group

    Alteration in methylation level at differential methylated regions of MEST and DLK1 in fetus of preeclampsia.
    Wang X, Wan L, Weng X, Xie J, Zhang A, Liu Y, Dong M.

    09/1/2018
    Some growth-regulating imprinted genes such as MEST and MEG3, are susceptible to non-imprinted allele during development and differentiation, whereas the intergenic differentially methylated region of others (i.e. PEG3) are strictly maintained.

    Hypermethylation of the non-imprinted maternal MEG3 and paternal MEST alleles is highly variable among normal individuals.
    Haertle L, Maierhofer A, Böck J, Lehnen H, Böttcher Y, Blüher M, Schorsch M, Potabattula R, El Hajj N, Appenzeller S, Haaf T., Free PMC Article

    10/21/2017
    strongly expressed in invasive extravillous trophoblasts during the first trimester

    DNA methylation-associated repression of MEST/PEG1 expression contributes to the invasion of extravillous trophoblast cells.
    Peng W, Chen Y, Luo X, Shan N, Lan X, Olson D, Zhang H, Ding YB, Qi HB.

    10/14/2017
    G4 formation at motifs not previously identified through bioinformatic analysis of the MEST promoter, is reported.

    Structural Analysis of G-Quadruplex Formation at the Human MEST Promoter.
    Stevens AJ, Kennedy MA., Free PMC Article

    08/12/2017
    altered DNA methylation at imprinted domains including IGF2/H19 and PEG1/MEST may mediate the association between human papillomavirus infection and invasive cervical cancer

    PEG1/MEST and IGF2 DNA methylation in CIN and in cervical cancer.
    Vidal AC, Henry NM, Murphy SK, Oneko O, Nye M, Bartlett JA, Overcash F, Huang Z, Wang F, Mlay P, Obure J, Smith J, Vasquez B, Swai B, Hernandez B, Hoyo C., Free PMC Article

    10/11/2014
    The expression levels of miR-335 significantly correlated with those of MEST, supporting the notion that the intronic miR-335 is co-expressed with its host gene

    Epigenetic silencing of miR-335 and its host gene MEST in hepatocellular carcinoma.
    Dohi O, Yasui K, Gen Y, Takada H, Endo M, Tsuji K, Konishi C, Yamada N, Mitsuyoshi H, Yagi N, Naito Y, Tanaka S, Arii S, Yoshikawa T., Free PMC Article

    01/11/2014
    DNA methylation level at the H19 and MEST differentially methylated regions (DMRs)is reduced in placentas from pregnancies conceived by IVF/ICSI when compared with placentas from spontaneous conception.

    Placentas from pregnancies conceived by IVF/ICSI have a reduced DNA methylation level at the H19 and MEST differentially methylated regions.
    Nelissen EC, Dumoulin JC, Daunay A, Evers JL, Tost J, van Montfoort AP.

    09/28/2013
    Paternal methylation aberrations at imprinting control regions of DLK1-GTL2, MEST (PEG1), and ZAC (PLAGL1) and global methylation levels are not associated with idiopathic recurrent spontaneous miscarriages.

    Methylation status of imprinted genes DLK1-GTL2, MEST (PEG1), ZAC (PLAGL1), and LINE-1 elements in spermatozoa of normozoospermic men, unlike H19 imprinting control regions, is not associated with idiopathic recurrent spontaneous miscarriages.
    Ankolkar M, Salvi V, Warke H, Vundinti BR, Balasinor NH.

    07/6/2013
    These results support the idea that intrauterine exposure to gestational diabetes mellitus has long-lasting effects on the epigenome of the offspring.

    Metabolic programming of MEST DNA methylation by intrauterine exposure to gestational diabetes mellitus.
    El Hajj N, Pliushch G, Schneider E, Dittrich M, Müller T, Korenkov M, Aretz M, Zechner U, Lehnen H, Haaf T., Free PMC Article

    05/25/2013
    Data indicate that ARMCX2, COL1A1, MDK, MEST and MLH1 genes acquired methylation in drug-resistant ovarian cancer-sustaining (side population) cells.

    Candidate DNA methylation drivers of acquired cisplatin resistance in ovarian cancer identified by methylome and expression profiling.
    Zeller C, Dai W, Steele NL, Siddiq A, Walley AJ, Wilhelm-Benartzi CS, Rizzo S, van der Zee A, Plumb JA, Brown R.

    01/26/2013
    MEST showed tissue-specific imprinting, being paternally expressed in skeletal muscle, fat, pituitary gland, heart, kidney, lung, stomach and uterus, and maternally expressed in spleen and liver.

    Conservation of genomic imprinting at the NDN, MAGEL2 and MEST loci in pigs.
    Zhang FW, Han ZB, Deng CY, He HJ, Wu Q.

    09/8/2012
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