2022
DOI: 10.2174/1389201022666210810100607
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The Prognostic Value of Long Non-Coding RNA SNHG7 in Human Cancer: A Meta-Analysis

Abstract: Background: The long non-coding RNA SNHG7 is upregulated in many types of cancer and plays a role as an oncogene. However, its overall predictive ability in human cancer prognosis has not been assessed using existing databases. Therefore, further study of its prognostic value and clinical significance in human malignancies is warranted. Methods: We systematically collected relevant literature from multiple electronic document databases about the relationship between SNHG7 expression level and prognosis in pa… Show more

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“…These include larger tumor size, more advanced clinical stage, poor histologic grade, deeper tumor invasion, and lymph node metastasis in accordance with high SNHG7 expression in the affected patients ( Zeng et al, 2019 ; Pang et al, 2020 ; Zhu et al, 2021 ). This value is also shown in malignancies with broad and different features and in meta-analyses pooling data of tens of studies ( Yu et al, 2021a ; Yi et al, 2021 ; Yu et al, 2021b ). For example, in acute myeloid leukemia (AML), an association between SNHG7 and SNHG12 lncRNAs and specific clinical/molecular features, including white blood cell (WBC) counts and mutations in IDH1 , RUNX1 , and NPM1 genes, shows high value of SNHG7 in correlation with extensive features ( Shi et al, 2020 ).…”
Section: Introductionmentioning
confidence: 63%
“…These include larger tumor size, more advanced clinical stage, poor histologic grade, deeper tumor invasion, and lymph node metastasis in accordance with high SNHG7 expression in the affected patients ( Zeng et al, 2019 ; Pang et al, 2020 ; Zhu et al, 2021 ). This value is also shown in malignancies with broad and different features and in meta-analyses pooling data of tens of studies ( Yu et al, 2021a ; Yi et al, 2021 ; Yu et al, 2021b ). For example, in acute myeloid leukemia (AML), an association between SNHG7 and SNHG12 lncRNAs and specific clinical/molecular features, including white blood cell (WBC) counts and mutations in IDH1 , RUNX1 , and NPM1 genes, shows high value of SNHG7 in correlation with extensive features ( Shi et al, 2020 ).…”
Section: Introductionmentioning
confidence: 63%