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pmid:38506098

Unveiling the role of YARS1 in bladder cancer: A prognostic biomarker and therapeutic target.

YaXuan Wang · Jinfeng Wang · Lu Zhang · JiaXing He · Bo Ji · JianShe Wang · BeiChen Ding · MingHua Ren

Journal of cellular and molecular medicine · 2024 doi:10.1111/jcmm.18213

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
Unveiling the role of YARS1 in bladder cancer: A prognostic biomarker and therapeutic target.
doi
10.1111/jcmm.18213
pmid
38506098
authors array · 8 items
[0]
YaXuan Wang
[1]
Jinfeng Wang
[2]
Lu Zhang
[3]
JiaXing He
[4]
Bo Ji
[5]
JianShe Wang
[6]
BeiChen Ding
[7]
MingHua Ren
journal
Journal of cellular and molecular medicine
year
2024
abstract
YARS is responsible for catalysing the binding of tyrosine to its cognate tRNA and plays a crucial role in basic biosynthesis. However, its biological functions in bladder cancer remains to be proven. We analysed variations in YARS1 expression and survival in bladder cancer using multiple data sets, including TCGA-BLCA, GSE13507 and bladder cancer-specific tissue microarrays. Furthermore, we explored the biological functions of YARS1 using transcriptome data. Our findings revealed a noteworthy correlation between YARS1 and immune infiltration in bladder cancer, as determined using the XCELL algorithm and single-cell analysis. In addition, we employed the TIDE algorithm to evaluate the responsiveness of different cohorts to immune checkpoint therapy. We investigated the regulatory associations between YARS1 and various aspects of bladder cancer, including senescence, ferroptosis and stemness. Finally, we established a ceRNA network that is directly linked to the overall prognosis, YARS1 can serve as a prognostic biomarker for bladder cancer; its interaction with MYC has implications for bladder cancer cell senescence, ferroptosis and stemness. Moreover, the identified ceRNA network has potential as a therapeutic target in bladder cancer.
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YARS1 expression in bladder cancer and normal bladder tissues was determined by the Wilcoxon rank‐sum test. Prognostic analysis was performed using the log‐rank test. Statistical significance was defined as p < 0.05.
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sections[10] "Statistical analysis" paragraph 2
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YARS1 expression in bladder cancer and normal bladder tissues was determined by the Wilcoxon rank‐sum test. Prognostic analysis was performed using the log‐rank test. Statistical significance was defined as p < 0.05.
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The data sets obtained from TCGA database (https://portal.gdc.cancer.gov/) and UALCAN database (http://ualcan.path.uab.edu/analysis.html), GEO database (https://www.ncbi.nlm.nih.gov/geo/), partial analysis by Cbioportal for Cancer Genomics website (http://www.cbioportal.org), TISCH (http://tisch.comp‐genomics.org/home/) database and SMART database (http://www.bioinfo‐zs.com/smartapp/).
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sections[28] "DATA AVAILABILITY STATEMENT" paragraph 2
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The data sets obtained from TCGA database (https://portal.gdc.cancer.gov/) and UALCAN database (http://ualcan.path.uab.edu/analysis.html), GEO database (https://www.ncbi.nlm.nih.gov/geo/), partial analysis by Cbioportal for Cancer Genomics website (http://www.cbioportal.org), TISCH (http://tisch.comp‐genomics.org/home/) database and SMART database (http://www.bioinfo‐zs.com/smartapp/).
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YARS1 was elevated in bladder carcinoma and was associated with an unfavourable prognosis.
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sections[13] "YARS1 can be used as a prognostic marker for bladder cancer" paragraph 2
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In conclusion, our investigation substantiates the elevated expression of YARS1 in bladder carcinoma and the unfavourable prognosis associated with this elevated expression.
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YARS1 was elevated in bladder carcinoma and was associated with an unfavourable prognosis.
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PMID 38506098 full text
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was obtained before the start of the study. Immunohistochemical analysis of YARS1 expression in bladder canc
[1]
hen subjected to a 20‐min incubation with an immunohistochemical secondary antibody at room temperature. Afte
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YARS1 expression in bladder cancer and normal bladder tissues was determined by the Wilcoxon rank‐sum test. Prognostic analysis was performed using the log‐rank test. Statistical significance was defined as p < 0.05.
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Complete file
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We analysed variations in YARS1 expression and survival in bladder cancer using multiple data sets, including TCGA-BLCA, GSE13507 and bladder cancer-specific tissue microarrays. Furthermore, we explored the biological functions of YARS1 using transcriptome data. Our findings revealed a noteworthy correlation between YARS1 and immune infiltration in bladder cancer, as determined using the XCELL algorithm and single-cell analysis. In addition, we employed the TIDE algorithm to evaluate the responsiveness of different cohorts to immune checkpoint therapy. We investigated the regulatory associations between YARS1 and various aspects of bladder cancer, including senescence, ferroptosis and stemness. Finally, we established a ceRNA network that is directly linked to the overall prognosis, YARS1 can serve as a prognostic biomarker for bladder cancer; its interaction with MYC has implications for bladder cancer cell senescence, ferroptosis and stemness. 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