Multi-omics analysis of N6-methyladenosine reader IGF2BP3 as a promising biomarker in pan-cancer

被引:7
作者
Chen, Pin [1 ]
Xu, Jing [2 ]
Cui, Zihan [3 ,4 ]
Wu, Silin [1 ]
Xie, Tao [1 ,5 ]
Zhang, Xiaobiao [1 ,5 ,6 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Neurosurg, Shanghai, Peoples R China
[2] Fudan Univ, Zhongshan Hosp, Dept Endocrinol & Metab, Shanghai, Peoples R China
[3] Soochow Univ, Affiliated Hosp 1, Med Coll, Dept Thorac Surg, Suzhou, Peoples R China
[4] Soochow Univ, Affiliated Hosp 1, Inst Thorac Surg, Suzhou, Peoples R China
[5] Fudan Univ, Shanghai Zhongshan Hosp, Canc Ctr, Shanghai, Peoples R China
[6] Fudan Univ, Digital Med Res Ctr, Shanghai, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
关键词
insulin-like growth factor 2 mRNA-binding protein 3 (IGF2BP3); pan-cancer analysis; genetic alteration; prognosis; the Cancer Genome Atlas (TCGA); immune infiltration; RNA-BINDING-PROTEIN; MARKER; PROGRESSION; INVASION; TRANSLATION; EXPRESSION; CARCINOMA; PROGNOSIS; SURVIVAL; TUMORS;
D O I
10.3389/fimmu.2023.1071675
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BackgroundInsulin-like growth factor 2 mRNA-binding protein 3 (IGF2BP3) has been reported to exhibit an oncogenic effect as an RNA-binding protein (RBP) by promoting tumor cell proliferation, migration and invasion in several tumor types. However, a pan-cancer analysis of IGF2BP3 is not currently available, and the exact roles of IGF2BP3 in prognosis and immunology in cancer patients remain enigmatic. The main aim of this study was to provide visualization of the systemic prognostic landscape of IGF2BP3 in pan-cancer and to uncover the potential relationship between IGF2BP3 expression in the tumor microenvironment and immune infiltration profile. MethodsRaw data on IGF2BP3 expression were obtained from GTEx, CCLE, TCGA, and HPA data portals. We have investigated the expression patterns, diagnostic and prognostic significance, mutation landscapes, functional analysis, and functional states of IGF2BP3 utilizing multiple databases, including HPA, TISIDB, cBioPortal, GeneMANIA, GESA, and CancerSEA. Moreover, the relationship of IGF2BP3 expression with immune infiltrates, TMB, MSI and immune-related genes was evaluated in pan-cancer. IGF2BP3 with drug sensitivity analysis was performed from the CellMiner database. Furthermore, the expression of IGF2BP3 in different grades of glioma was detected by immunohistochemical staining and western blot. ResultsWe found that IGF2BP3 was ubiquitously highly expressed in pan-cancer and significantly correlated with diagnosis, prognosis, TMB, MSI, and drug sensitivity in various types of cancer. Besides, IGF2BP3 was involved in many cancer pathways and varied in different immune and molecular subtypes of cancers. Additionally, IGF2BP3 is critically associated with genetic markers of immunomodulators in various cancers. Finally, we validated that IGF2BP3 protein expression was significantly higher in glioma than in normal tissue, especially in GBM. ConclusionsIGF2BP3 may be a potential molecular biomarker for diagnosis and prognosis in pan-cancer, especially for glioma. It could become a novel therapeutic target for various cancers.
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页数:23
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共 75 条
  • [41] Nielsen J, 1999, MOL CELL BIOL, V19, P1262
  • [42] International validation of the consensus Immunoscore for the classification of colon cancer: a prognostic and accuracy study
    Pages, Franck
    Mlecnik, Bernhard
    Marliot, Florence
    Bindea, Gabriela
    Ou, Fang-Shu
    Bifulco, Carlo
    Lugli, Alessandro
    Zlobec, Inti
    Rau, Tilman T.
    Berger, Martin D.
    Nagtegaal, Iris D.
    Vink-Borger, Elisa
    Hartmann, Arndt
    Geppert, Carol
    Kolwelter, Julie
    Merkel, Susanne
    Gruetzmann, Robert
    Van den Eynde, Marc
    Jouret-Mourin, Anne
    Kartheuser, Alex
    Leonard, Daniel
    Remue, Christophe
    Wang, Julia Y.
    Bavi, Prashant
    Roehrl, Michael H. A.
    Ohashi, Pamela S.
    Nguyen, Linh T.
    Han, SeongJun
    MacGregor, Heather L.
    Hafezi-Bakhtiari, Sara
    Wouters, Bradly G.
    Masucci, Giuseppe V.
    Andersson, Emilia K.
    Zavadova, Eva
    Vocka, Michal
    Spacek, Jan
    Petruzelka, Lubos
    Konopasek, Bohuslav
    Dundr, Pavel
    Skalova, Helena
    Nemejcova, Kristyna
    Botti, Gerardo
    Tatangelo, Fabiana
    Delrio, Paolo
    Ciliberto, Gennaro
    Maio, Michele
    Laghi, Luigi
    Grizzi, Fabio
    Fredriksen, Tessa
    Buttard, Benedicte
    [J]. LANCET, 2018, 391 (10135) : 2128 - 2139
  • [43] IMP-3 is a novel progression marker in malignant melanoma
    Pryor, Jennifer G.
    Bourne, Patricia A.
    Yang, Qi
    Spaulding, Betsy O.
    Scott, Glynis A.
    Xu, Haodong
    [J]. MODERN PATHOLOGY, 2008, 21 (04) : 431 - 437
  • [44] CellMiner: A Web-Based Suite of Genomic and Pharmacologic Tools to Explore Transcript and Drug Patterns in the NCI-60 Cell Line Set
    Reinhold, William C.
    Sunshine, Margot
    Liu, Hongfang
    Varma, Sudhir
    Kohn, Kurt W.
    Morris, Joel
    Doroshow, James
    Pommier, Yves
    [J]. CANCER RESEARCH, 2012, 72 (14) : 3499 - 3511
  • [45] Tumor and Microenvironment Evolution during Immunotherapy with Nivolumab
    Riaz, Nadeem
    Havel, Jonathan J.
    Makarov, Vladimir
    Desrichard, Alexis
    Urba, Walter J.
    Sims, Jennifer S.
    Hodi, F. Stephen
    Martin-Algarra, Salvador
    Mandal, Rajarsi
    Sharfman, William H.
    Bhatia, Shailender
    Hwu, Wen-Jen
    Gajewski, Thomas F.
    Slingluff, Craig L., Jr.
    Chowell, Diego
    Kendall, Sviatoslav M.
    Chang, Han
    Shah, Rachna
    Kuo, Fengshen
    Morris, Luc G. T.
    Sidhom, John-William
    Schneck, Jonathan P.
    Horak, Christine E.
    Weinhold, Nils
    Chan, Timothy A.
    [J]. CELL, 2017, 171 (04) : 934 - +
  • [46] Mutational landscape determines sensitivity to PD-1 blockade in non-small cell lung cancer
    Rizvi, Naiyer A.
    Hellmann, Matthew D.
    Snyder, Alexandra
    Kvistborg, Pia
    Makarov, Vladimir
    Havel, Jonathan J.
    Lee, William
    Yuan, Jianda
    Wong, Phillip
    Ho, Teresa S.
    Miller, Martin L.
    Rekhtman, Natasha
    Moreira, Andre L.
    Ibrahim, Fawzia
    Bruggeman, Cameron
    Gasmi, Billel
    Zappasodi, Roberta
    Maeda, Yuka
    Sander, Chris
    Garon, Edward B.
    Merghoub, Taha
    Wolchok, Jedd D.
    Schumacher, Ton N.
    Chan, Timothy A.
    [J]. SCIENCE, 2015, 348 (6230) : 124 - 128
  • [47] Targeting the Raf-MEK-ERK mitogen-activated protein kinase cascade for the treatment of cancer
    Roberts, P. J.
    Der, C. J.
    [J]. ONCOGENE, 2007, 26 (22) : 3291 - 3310
  • [48] Molecular and Genetic Properties of Tumors Associated with Local Immune Cytolytic Activity
    Rooney, Michael S.
    Shukla, Sachet A.
    Wu, Catherine J.
    Getz, Gad
    Hacohen, Nir
    [J]. CELL, 2015, 160 (1-2) : 48 - 61
  • [49] TISIDB: an integrated repository portal for tumor-immune system interactions
    Ru, Beibei
    Wong, Ching Ngar
    Tong, Yin
    Zhong, Jia Yi
    Zhong, Sophia Shek Wa
    Wu, Wai Chung
    Chu, Ka Chi
    Wong, Choi Yiu
    Lau, Chit Ying
    Chen, Ian
    Chan, Nam Wai
    Zhang, Jiangwen
    [J]. BIOINFORMATICS, 2019, 35 (20) : 4200 - 4202
  • [50] PD-L1 expression, tumor mutational burden, and response to immunotherapy in patients with MET exon 14 altered lung cancers
    Sabari, J. K.
    Leonardi, G. C.
    Shu, C. A.
    Umeton, R.
    Montecalvo, J.
    Ni, A.
    Chen, R.
    Dienstag, J.
    Mrad, C.
    Bergagnini, I.
    Lai, W. V.
    Offin, M.
    Arbour, K. C.
    Plodkowski, A. J.
    Halpenny, D. F.
    Paik, P. K.
    Li, B. T.
    Riely, G. J.
    Kris, M. G.
    Rudin, C. M.
    Sholl, L. M.
    Nishino, M.
    Hellmann, M. D.
    Rekhtman, N.
    Awad, M. M.
    Drilon, A.
    [J]. ANNALS OF ONCOLOGY, 2018, 29 (10) : 2085 - 2091