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Gene & Protein in Disease                                     Exploring serum inflammatory biomarkers in GBM



            (ii)  Statistical significance may be observed in specific   NIH intramural IRB is IRB00011862. Informed consent
               patient sub-cohorts, e.g., patients with methylated   was obtained for all subjects before this study.
               MGMT or larger tumor burdens.
            (iii) IL-6 may have mechanistic links with other statistically   Consent for publication
               significant markers, as noted in this analysis, where   All subjects gave consent to publish their data in this study.
               it  emerged as  a  dominant  functional  unit in  IPA
               pathways.                                       Availability of data
            (iv)  IL-6 may play critical functional roles but exhibit   Responsible data sharing is part of our mandate and the
               divergent behavior in patient cohorts, e.g., patients   cardinal future direction of this dataset. We are currently
               with more radio-  or chemo-resistant disease,   aggregating  several  data  aspects  including  additional
               suggesting that its significance may only become
               apparent when adjusting for specific clinical features   samples and omic data and once this is complete, the set
               in future analyses.                             will be de-identified and shared. The goal is to provide one
                                                               comprehensive GBM dataset that has clinical, omic, and
              Further  research  is  needed  to  understand  how  IL-6   imaging data. Individual requests to access the datasets
            may function as a potential driver of the observed signal   should be directed to the corresponding author.
            alterations and how these are linked to APR pathways.
            The role  of IL-6 as  a possible mediator of tumor   References
            microenvironment reprogramming, in conjunction with   1.   Hanif F, Muzaffar  K, Perveen K,  Malhi SM,  Simjee  SU.
            TNF-α and VCAM-1, requires larger data sets and the   Glioblastoma multiforme: A review of its epidemiology and
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            proliferative, and pro-viability pathways through STAT3      doi: 10.22034/apjcp.2017.18.1.3
            and NF-κB pathways, which may serve as potential
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                                                                  doi: 10.1073/pnas.1219747110
            Acknowledgments                                    3.   Dehdashti AR, Hegi ME, Regli L, Pica A, Stupp R. New trends
            None.                                                 in the medical management of glioblastoma multiforme:
                                                                  The role of temozolomide chemotherapy. Neurosurg Focus.
            Funding                                               2006;20(4):E6.

            Funding is provided in part by the NCI NIH intramural      doi: 10.3171/foc.2006.20.4.3
            program (ZID BC 010990).                           4.   McKelvey KJ, Hudson AL, Back M, Eade T, Diakos CI.
                                                                  Radiation, inflammation and the immune response in
            Conflict of interest                                  cancer. Mamm Genome. 2018;29(11-12):843-865.
            The authors declare that they have no competing interests.     doi: 10.1007/s00335-018-9777-0

            Author contributions                               5.   Serban GM, Tamas CI, Tamas F, Balasa AF. preoperative
                                                                  immune-inflammatory  status  of the  patients with newly-
            Conceptualization: Sarisha Jagasia, Andra V. Krauze   diagnosed glioblastoma  -  could it genuinely predict their
            Investigation:  Sarisha Jagasia, Jason Shephard, Andra V.   survival? Cureus. 2023;15(8):e43802.
               Krauze                                             doi: 10.7759/cureus.43802
            Methodology: Sarisha Jagasia, Andra V. Krauze
            Writing – original draft: Sarisha Jagasia, Andra V. Krauze   6.   Knebel FH, Uno M, Galatro TF, et al. Serum amyloid A1
                                                                  is upregulated in human glioblastoma.  J  Neurooncol.
            Writing – review & editing: All authors               2017;132(3):383-391.
            Ethics approval and consent to participate            doi: 10.1007/s11060-017-2386-z

            Most of the GBM patients involved in this study are   7.   Linhares P, Carvalho B, Vaz R, Costa BM. Glioblastoma: Is
            deceased; however, all patients were treated on NCI NIH   there any blood biomarker with true clinical relevance? Int J
            IRB-approved protocols, and there is no identifiable   Mol Sci. 2020;21(16):5809.
            information present in the article. The IRB number for the      doi: 10.3390/ijms21165809


            Volume 3 Issue 3 (2024)                         13                              doi: 10.36922/gpd.3580
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