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LncRNA FOXD3-AS1/miR-128-3p axis-mediated IGF2BP3 in glioma stimulates cancer angiogenesis and progression

Zhao, Hongxin, Wang, Yuyu, Liang, Chuandong, Xie, Mingxiang·2023·Folia Neuropathologica

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Fig. 1 IGF2BP3 is highly expressed in glioma. A ) Volcano plot of DEmRNAs in normal and tumour groups. B ) IGF2BP3 expression in glioma tissue and normal tissue. Y-axis: mRNA expression, X-axis: sample type. C ) Survival analysis tested the relationship between IGF2BP3 level and patient's prognosis. Blue: low expression, red: high expression. D, E ) IGF2BP3 mRNA and protein expression in HEB, T98G, U87 and U251 cell lines, respectively. * p < 0.05.
Fig. 1 IGF2BP3 is highly expressed in glioma. A ) Volcano plot of DEmRNAs in normal and tumour groups. B ) IGF2BP3 expression in glioma tissue and normal tissue. Y-axis: mRNA expression, X-axis: sample type. C ) Survival analysis tested the relationship between IGF2BP3 level and patient's prognosis. Blue: low expression, red: high expression. D, E ) IGF2BP3 mRNA and protein expression in HEB, T98G, U87 and U251 cell lines, respectively. * p < 0.05.CC-BY-NC-SA · From the PDF
Fig. 2 Silencing IGF2BP3 suppresses growth of glioma cells. A, B ) IGF2BP3 mRNA and protein levels in U87 and U251 cells upon silencing IGF2BP3. C ) The viability of tumour cells regulated by IGF2BP3. D ) The impact of silencing IGF2BP3 on colony formative ability of tumour cells. E ) The inhibition of silencing IGF2BP3 on migration of tumour cells (100×).
Fig. 2 Silencing IGF2BP3 suppresses growth of glioma cells. A, B ) IGF2BP3 mRNA and protein levels in U87 and U251 cells upon silencing IGF2BP3. C ) The viability of tumour cells regulated by IGF2BP3. D ) The impact of silencing IGF2BP3 on colony formative ability of tumour cells. E ) The inhibition of silencing IGF2BP3 on migration of tumour cells (100×).CC-BY-NC-SA · From the PDF
Fig. 2 Cont. F ) The invasive ability of tumour cells by silencing IGF2BP3 expression (100×). G ) IGF2BP3 knockdown influences tube formation in glioma. * p < 0.05.
Fig. 2 Cont. F ) The invasive ability of tumour cells by silencing IGF2BP3 expression (100×). G ) IGF2BP3 knockdown influences tube formation in glioma. * p < 0.05.CC-BY-NC-SA · From the PDF
Fig. 3 miR-128-3p restrains IGF2BP3 expression in glioma. A ) Volcano plot of DEmiRNAs in normal and tumour groups. Green: downregulated genes, red: upregulated genes. B ) Venn diagram of target mRNAs and downregulated DEmiRNAs. C ) Scatter plot of correlation between miR-128-3p and IGF2BP3. D ) Violin plot of miR-128-3p level in normal (blue) and tumour group (red). E ) Survival curve of miR-128-3p on prognosis. Blue: low expression, red: high expression. F ) MiR-128-3p expression in glioma cells. G, H ) The impact of overexpressing miR-1283p on IGF2BP3 mRNA and protein levels in U87 cells and U251 cells. I ) Binding sites between miR-128-3p and IGF2BP3. J ) Validating the binding between miR-128-3p and IGF2BP3. * p < 0.05.
Fig. 3 miR-128-3p restrains IGF2BP3 expression in glioma. A ) Volcano plot of DEmiRNAs in normal and tumour groups. Green: downregulated genes, red: upregulated genes. B ) Venn diagram of target mRNAs and downregulated DEmiRNAs. C ) Scatter plot of correlation between miR-128-3p and IGF2BP3. D ) Violin plot of miR-128-3p level in normal (blue) and tumour group (red). E ) Survival curve of miR-128-3p on prognosis. Blue: low expression, red: high expression. F ) MiR-128-3p expression in glioma cells. G, H ) The impact of overexpressing miR-1283p on IGF2BP3 mRNA and protein levels in U87 cells and U251 cells. I ) Binding sites between miR-128-3p and IGF2BP3. J ) Validating the binding between miR-128-3p and IGF2BP3. * p < 0.05.CC-BY-NC-SA · From the PDF
Fig. 4 MiR-128-3p targets IGF2BP3 to repress glioma progression. A ) IGF2BP expression in different transfected cells. B ) MiR-128-3 p/IGF2BP3 axis impact on U87 and U251 cell viability. C ) Colony formation of U87 and U251 cells in each treatment group. D ) The regulatory role of miR-128-3p and IGF2BP3 in glioma cell migration (100×).
Fig. 4 MiR-128-3p targets IGF2BP3 to repress glioma progression. A ) IGF2BP expression in different transfected cells. B ) MiR-128-3 p/IGF2BP3 axis impact on U87 and U251 cell viability. C ) Colony formation of U87 and U251 cells in each treatment group. D ) The regulatory role of miR-128-3p and IGF2BP3 in glioma cell migration (100×).CC-BY-NC-SA · From the PDF
Fig. 4 Cont. E ) The regulatory role of miR-128-3p and IGF2BP3 in glioma cell invasion (100×). F ) MiR-128-3p and IGF2BP influence glioma angiogenesis. * p < 0.05.
Fig. 4 Cont. E ) The regulatory role of miR-128-3p and IGF2BP3 in glioma cell invasion (100×). F ) MiR-128-3p and IGF2BP influence glioma angiogenesis. * p < 0.05.CC-BY-NC-SA · From the PDF
Fig. 5 FOXD3-AS1 stimulates IGF2BP3 level via miR-128-3p inhibition. A ) Volcano plot of DElncRNAs in normal and tumour groups. Green: downregulated DElncRNAs, red: upregulated DElncRNAs. B ) Venn diagram of predicted lncRNAs and upregulated DElncRNAs. C ) Heat map of correlation between candidate lncRNAs and IGF2BP3. D ) Violin plot of FOXD3-AS1 level in the normal group (blue) and the tumour group (red). E ) Survival curve of prognosis of patients with different FOXD3-AS1 expressions. Red: high expression, blue: low expression. F ) FOXD3-AS1 level in normal cells and glioma cells. G ) Expression sites of FOXD3-AS1 in glioma cells. H ) Binding sequences of FOXD3-AS1 and miR-128-3p. I ) The targeting between FOXD3-AS1 and miR-128-3p. J ) The impact of silencing FOXD3-AS1 on miR-128-3p expression. * p < 0.05.
Fig. 5 FOXD3-AS1 stimulates IGF2BP3 level via miR-128-3p inhibition. A ) Volcano plot of DElncRNAs in normal and tumour groups. Green: downregulated DElncRNAs, red: upregulated DElncRNAs. B ) Venn diagram of predicted lncRNAs and upregulated DElncRNAs. C ) Heat map of correlation between candidate lncRNAs and IGF2BP3. D ) Violin plot of FOXD3-AS1 level in the normal group (blue) and the tumour group (red). E ) Survival curve of prognosis of patients with different FOXD3-AS1 expressions. Red: high expression, blue: low expression. F ) FOXD3-AS1 level in normal cells and glioma cells. G ) Expression sites of FOXD3-AS1 in glioma cells. H ) Binding sequences of FOXD3-AS1 and miR-128-3p. I ) The targeting between FOXD3-AS1 and miR-128-3p. J ) The impact of silencing FOXD3-AS1 on miR-128-3p expression. * p < 0.05.CC-BY-NC-SA · From the PDF
Fig. 5 Cont. K ) FOXD3-AS1, miR-128-3p and IGF2BP3 mRNA levels in cells. * p < 0.05.
Fig. 5 Cont. K ) FOXD3-AS1, miR-128-3p and IGF2BP3 mRNA levels in cells. * p < 0.05.CC-BY-NC-SA · From the PDF
Fig. 6 FOXD3-AS1 stimulates malignant growth of glioma cells via the miR-128-3p/IGF2BP3 axis. A ) Proliferation ability of glioma cells in different groups. B ) The colony formation of glioma cells. C ) The impact of different treatments on migration ability of U87 and U251 cells (100×) * p < 0.05.
Fig. 6 FOXD3-AS1 stimulates malignant growth of glioma cells via the miR-128-3p/IGF2BP3 axis. A ) Proliferation ability of glioma cells in different groups. B ) The colony formation of glioma cells. C ) The impact of different treatments on migration ability of U87 and U251 cells (100×) * p < 0.05.CC-BY-NC-SA · From the PDF
Fig. 6 Cont. D ) The impact of FOXD3-AS1, miR-128-3p and IGF2BP3 on invasion ability of glioma U87 and U251 (100×). E ) Angiogenesis of glioma cells. * p < 0.05.
Fig. 6 Cont. D ) The impact of FOXD3-AS1, miR-128-3p and IGF2BP3 on invasion ability of glioma U87 and U251 (100×). E ) Angiogenesis of glioma cells. * p < 0.05.CC-BY-NC-SA · From the PDF
Fig. 7 Silencing IGF2BP3 inhibits tumour growth of nude mice glioma in vivo . A ) Xenograft nude mice tumour growth weight in si-NC or si-IGF2BP3 in U87 cells. Mean ± standard deviation ( n = 6/group). B ) Tumour volume of glioma in si-NC and si-IGF2BP3 groups. C ) The positive expression rates of IGF2BP3 and Ki67 in tumour tissue of nude mice after IGF2BP3 silencing (400×). D ) IGF2BP3 mRNA and protein levels in tumour tissues of nude mice. * p < 0.05.
Fig. 7 Silencing IGF2BP3 inhibits tumour growth of nude mice glioma in vivo . A ) Xenograft nude mice tumour growth weight in si-NC or si-IGF2BP3 in U87 cells. Mean ± standard deviation ( n = 6/group). B ) Tumour volume of glioma in si-NC and si-IGF2BP3 groups. C ) The positive expression rates of IGF2BP3 and Ki67 in tumour tissue of nude mice after IGF2BP3 silencing (400×). D ) IGF2BP3 mRNA and protein levels in tumour tissues of nude mice. * p < 0.05.CC-BY-NC-SA · From the PDF

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Research works printed but not linked: 46

  1. Bello L, Giussani C, Carrabba G, Pluderi M, Costa F, Bikfalvi A. Angiogenesis and invasion in gliomas. Cancer Treat Res 2004; 117: 263-284.
  2. Bhan A, Soleimani M, Mandal SS. Long noncoding RNA and cancer: A new paradigm. Cancer Res 2017; 77: 3965-3981.
  3. Bhargava S, Patil V, Shah RA, Somasundaram K. IGF2 mRNA binding protein 3 (IMP3) mediated regulation of transcriptome and translatome in glioma cells. Cancer Biol Ther 2018; 19: 42-52.
  4. Burdelski C, Jakani-Karimi N, Jacobsen F, Moller-Koop C, Minner S, Simon R, Sauter G, Steurer S, Clauditz TS, Wilczak W. IMP3 overexpression occurs in various important cancer types and is linked to aggressive tumor features: A tissue microarray study on 8,877 human cancers and normal tissues. Oncol Rep 2018; 39: 3-12.
  5. Chen ZH, Hu HK, Zhang CR, Lu CY, Bao Y, Cai Z, Zou YX, Hu GH, Jiang L. Down-regulation of long non-coding RNA FOXD3 anti- sense RNA 1 (FOXD3-AS1) inhibits cell proliferation, migration, and invasion in malignant glioma cells. Am J Transl Res 2016; 8: 4106-4119.
  6. Dong D, Mu Z, Wei N, Sun M, Wang W, Xin N, Shao Y, Zhao C. Long non-coding RNA ZFAS1 promotes proliferation and metas- tasis of clear cell renal cell carcinoma via targeting miR-10a/ SKA1 pathway. Biomed Pharmacother 2019; 111: 917-925.
  7. Fu C, Li D, Zhang X, Liu N, Chi G, Jin X. LncRNA PVT1 facilitates tumorigenesis and progression of glioma via regulation of MiR- 128-3p/GREM1 axis and BMP signaling pathway. Neurothera- peutics 2018; 15: 1139-1157.
  8. Griveau A, Seano G, Shelton SJ, Kupp R, Jahangiri A, Obernier K, Krishnan S, Lindberg OR, Yuen TJ, Tien AC, Sabo JK, Wang N, Chen I, Kloepper J, Larrouquere L, Ghosh M, Tirosh I, Huillard E, Alvarez-Buylla A, Oldham MC, Persson AI, Weiss WA, Batche- lor TT, Stemmer-Rachamimov A, Suvà ML, Phillips JJ, Aghi MK, Mehta S, Jain RK, Rowitch DH. A glial signature and Wnt7 sig- naling regulate glioma-vascular interactions and tumor micro- environment. Cancer Cell 2018; 33: 874-889.e877.
  9. Hanniford D, Ulloa-Morales A, Karz A, Berzoti-Coelho MG, Mou- barak RS, Sanchez-Sendra B, Kloetgen A, Davalos V, Imig J, Wu P, Vasudevaraja V, Argibay D, Lilja K, Tabaglio T, Monteagudo C, Guccione E, Tsirigos A, Osman I, Aifantis I, Hernando E. Epigen- etic silencing of CDR1as drives IGF2BP3-mediated melanoma invasion and metastasis. Cancer Cell 2020; 37: 55-70.e15.
  10. Hartmann EM, Bea S, Navarro A, Trapp V, Campo E, Ott G, Ros- enwald A. Increased tumor cell proliferation in mantle cell lym- phoma is associated with elevated insulin-like growth factor 2 mRNA-binding protein 3 expression. Mod Pathol 2012; 25: 1227-1235.
  11. 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 gli- oma via miR-103a-3p/miR-382-5p mediated ZIC4 expression change. J Exp Clin Cancer Res 2019; 38: 9.
  12. Hsu KF, Shen MR, Huang YF, Cheng YM, Lin SH, Chow NH, Cheng SW, Chou CY, Ho CL. Overexpression of the RNA-bind- ing proteins Lin28B and IGF2BP3 (IMP3) is associated with chemoresistance and poor disease outcome in ovarian cancer. Br J Cancer 2015; 113: 414-424.
  13. Huo L, Wang B, Zheng M, Zhang Y, Xu J, Yang G, Guan Q. miR-128-3p inhibits glioma cell proliferation and differentiation by targeting NPTX1 through IRS-1/PI3K/AKT signaling pathway. Exp Ther Med 2019; 17: 2921-2930.
  14. Jain RK, di Tomaso E, Duda DG, Loeffler JS, Sorensen AG, Batch- elor TT. Angiogenesis in brain tumours. Nat Rev Neurosci 2007; 8: 610-622.
  15. Jeng YM, Chang CC, Hu FC, Chou HY, Kao HL, Wang TH, Hsu HC. RNA-binding protein insulin-like growth factor II mRNA-bind- ing protein 3 expression promotes tumor invasion and predicts early recurrence and poor prognosis in hepatocellular carcino- ma. Hepatology 2008; 48: 1118-1127.
  16. Jiang H, Liang M, Jiang Y, Zhang T, Mo K, Su S, Wang A, Zhu Y, Huang G, Zhou R. The lncRNA TDRG1 promotes cell prolifera- tion, migration and invasion by targeting miR-326 to regulate MAPK1 expression in cervical cancer. Cancer Cell Int 2019; 19: 152.
  17. Jiang L, Li Y, He Y, Wei D, Yan L, Wen H. Knockdown of m6A read- er IGF2BP3 inhibited hypoxia-induced cell migration and angio- genesis by regulating hypoxia inducible factor-1α in stomach cancer. Front Oncol 2021; 11: 711207.
  18. Jin P, Huang Y, Zhu P, Zou Y, Shao T, Wang O. CircRNA circHIPK3 serves as a prognostic marker to promote glioma progression by regulating miR-654/IGF2BP3 signaling. Biochem Biophys Res Commun 2018; 503: 1570-1574.
  19. Kobel M, Xu H, Bourne PA, Spaulding BO, Shih Ie M, Mao TL, Soslow RA, Ewanowich CA, Kalloger SE, Mehl E, Lee CH, Hunts- man D, Gilks CB. IGF2BP3 (IMP3) expression is a marker of unfa- vorable prognosis in ovarian carcinoma of clear cell subtype. Mod Pathol 2009; 22: 469-475.
  20. Kouhkan F, Mobarra N, Soufi-Zomorrod M, Keramati F, Hosseini Rad SM, Fathi-Roudsari M, Tavakoli R, Hajarizadeh A, Ziaei S, Lahmi R, Hanif H, Soleimani M. MicroRNA-129-1 acts as tumour suppressor and induces cell cycle arrest of GBM cancer cells through targeting IGF2BP3 and MAPK1. J Med Genet 2016; 53: 24-33.
  21. Li Z, Li M, Xia P, Wang L, Lu Z. LncRNA FOXD3-AS1 promotes tumorigenesis of glioma via targeting miR-128-3p/SZRD1 axis. Cancer Manag Res 2021; 13: 9037-9048.
  22. Liu G, Jiang R, Xu C, Zhou J, Liu F, He Z, Liu Z. Survival analysis for high-grade glioma patients who received comprehensive treatment. Zhong Nan Da Xue Xue Bao Yi Xue Ban 2018; 43: 388-393.
  23. Liu H, Zeng Z, Afsharpad M, Lin C, Wang S, Yang H, Liu S, Kele- men LE, Xu W, Ma W, Xiang Q, Mastriani E, Wang P, Wang J, Liu SL, Johnston RN, Kobel M. Overexpression of IGF2BP3 as a potential oncogene in ovarian clear cell carcinoma. Front Oncol 2019; 9: 1570.
  24. Liu T, Zhang X, Du L, Wang Y, Liu X, Tian H, Wang L, Li P, Zhao Y, Duan W, Xie Y, Sun Z, Wang C. Exosome-transmitted miR-128- 3p increase chemosensitivity of oxaliplatin-resistant colorectal cancer. Mol Cancer 2019; 18: 43.
  25. Liu X, Dong C, Ma S, Wang Y, Lin T, Li Y, Yang S, Zhang W, Zhang R, Zhao G. Nanocomplexes loaded with miR-128-3p for enhanc- ing chemotherapy effect of colorectal cancer through dual-tar- geting silence the activity of PI3K/AKT and MEK/ERK pathway. Drug Deliv 2020; 27: 323-333.
  26. Mancarella C, Scotlandi K. IGF2BP3 from physiology to cancer: novel discoveries, unsolved issues, and future perspectives. Front Cell Dev Biol 2019; 7: 363.
  27. Meng P, Ma S, Liu Y, Zhao N, Xia X, Bi Y. MiR-128-3p targets JAG1 to inhibit cell proliferation and invasion in melanoma. Ital J Der- matol Venerol 2021; 156: 250-251.
  28. Moncayo G, Grzmil M, Smirnova T, Zmarz P, Huber RM, Hynx D, Kohler H, Wang Y, Hotz HR, Hynes NE, Keller G, Frank S, Merlo A, Hemmings BA. SYK inhibition blocks proliferation and migra- tion of glioma cells and modifies the tumor microenvironment. Neuro Oncol 2018; 20: 621-631.
  29. Nielsen FC, Nielsen J, Christiansen J. A family of IGF-II mRNA binding proteins (IMP) involved in RNA trafficking. Scand J Clin Lab Invest Suppl 2001; 234: 93-99.
  30. Omuro A, DeAngelis LM. Glioblastoma and other malignant gli- omas: a clinical review. JAMA 2013; 310: 1842-1850.
  31. Peng Z, Liu C, Wu M. New insights into long noncoding RNAs and their roles in glioma. Mol Cancer 2018; 17: 61.
  32. Qu C, Yan C, Cao W, Li F, Qu Y, Guan K, Si C, Yu Z, Qu Z. miR- 128-3p contributes to mitochondrial dysfunction and induces apoptosis in glioma cells via targeting pyruvate dehydrogenase kinase 1. IUBMB Life 2020; 72: 465-475.
  33. Ren Y, Shang J, Li J, Liu W, Zhang Z, Yuan J, Yang M. The long noncoding RNA PCAT-1 links the microRNA miR-215 to onco- gene CRKL-mediated signaling in hepatocellular carcinoma. J Biol Chem 2017; 292: 17939-17949.
  34. Samanta S, Sharma VM, Khan A, Mercurio AM. Regulation of IMP3 by EGFR signaling and repression by ERbeta: implications for triple-negative breast cancer. Oncogene 2012; 31: 4689- 4697.
  35. Shantha Kumara H, Kirchoff D, Caballero OL, Su T, Ahmed A, Herath SA, Njoh L, Cekic V, Simpson AJ, Cordon-Cardo C, Whel- an RL. Expression of the cancer testis antigen IGF2BP3 in col- orectal cancers; IGF2BP3 holds promise as a specific immuno- therapy target. Oncoscience 2015; 2: 607-614.
  36. Suvasini R, Shruti B, Thota B, Shinde SV, Friedmann-Morvinski D, Nawaz Z, Prasanna KV, Thennarasu K, Hegde AS, Arivazhagan A, Chandramouli BA, Santosh V, Somasundaram K. Insulin growth factor-2 binding protein 3 (IGF2BP3) is a glioblastoma-specif- ic marker that activates phosphatidylinositol 3-kinase/mito- gen-activated protein kinase (PI3K/MAPK) pathways by mod- ulating IGF-2. J Biol Chem 2011; 286: 25882-25890.
  37. Taylor LP. Diagnosis, treatment, and prognosis of glioma: five new things. Neurology 2010; 75: S28-32.
  38. Valadez JG, Sarangi A, Lundberg CJ, Cooper MK. Primary orthotopic glioma xenografts recapitulate infiltrative growth and isocitrate dehydrogenase I mutation. J Vis Exp 2014; 83: e50865.
  39. Yang X, Du H, Bian W, Li Q, Sun H. FOXD3AS1/miR1283p/LIMK1 axis regulates cervical cancer progression. Oncol Rep 2021; 45: 62.
  40. Yang Z, Wang T, Wu D, Min Z, Tan J, Yu B. RNA N6-methylade- nosine reader IGF2BP3 regulates cell cycle and angiogenesis in colon cancer. J Exp Clin Cancer Res 2020; 39: 203.
  41. Zeng ZL, Zhu HK, He LF, Xu X, Xie A, Zheng EK, Ni JJ, Liu JT, Zhao GF. Highly expressed lncRNA FOXD3-AS1 promotes non- small cell lung cancer progression via regulating miR-127-3p/ mediator complex subunit 28 axis. Eur Rev Med Pharmacol Sci 2020; 24: 2525-2538.
  42. Zhang J, Ding F, Jiao D, Li Q, Ma H. The aberrant expression of microRNA-125a-5p/IGF2BP3 axis in advanced gastric cancer and its clinical relevance. Technol Cancer Res Treat 2020; 19: 1533033820917332.
  43. Zhang Y, Guo S, Wang S, Li X, Hou D, Li H, Wang L, Xu Y, Ma B, Wang H, Jiang X. LncRNA OIP5-AS1 inhibits ferroptosis in pros- tate cancer with long-term cadmium exposure through miR- 128-3p/SLC7A11 signaling. Ecotoxicol Environ Saf 2021; 220: 112376.
  44. Zhao W, Lu D, Liu L, Cai J, Zhou Y, Yang Y, Zhang Y, Zhang J. Insu- lin-like growth factor 2 mRNA binding protein 3 (IGF2BP3) pro- motes lung tumorigenesis via attenuating p53 stability. Onco- target 2017; 8: 93672-93687.
  45. Zhou X, He J, Wang Q, Ma T. MiRNA-128-3p restrains malignant melanoma cell malignancy by targeting NTRK3. Front Oncol 2020; 10: 538894.
  46. Zhu L, Wang A, Gao M, Duan X, Li Z. LncRNA MIR4435-2HG triggers ovarian cancer progression by regulating miR-128-3p/ CKD14 axis. Cancer Cell Int 2020; 20: 145.

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Authors
Zhao, H., Wang, Y., Liang, C., & Xie, M.
Venue
Folia Neuropathologica
Published
2023
Volume
61
Issue
2
Pages
168-184
ISSN
1641-4640
Cited by
9
References
0

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