Abstract:Background: Glycolysis is critical in the occurrence and development of tumors. Owing to the biological and clinical heterogeneity of patients with BRCA, the traditional predictive classification system is far from satisfactory. Survival and prognosis biomarkers related to glycolysis have broad application prospects for assessing the risk of patients and guiding their individualized treatment.Methods: The mRNA expression profiles and clinical information of patients with BRCA were obtained from TCGA database, … Show more
“…5 ), suggesting that PFKL is an attracting therapeutic target for cancer treatment. Our findings were corroborated by the recent studies showing that PFKL is upregulated in breast cancer and liver cancer 3 , and associated with patient survival 47 , 48 . In our study, a combination of DARTS technology and mass spectrometry-based proteomics, as well as SPR assay, revealed the direct binding of penfluridol to PFKL.…”
“…5 ), suggesting that PFKL is an attracting therapeutic target for cancer treatment. Our findings were corroborated by the recent studies showing that PFKL is upregulated in breast cancer and liver cancer 3 , and associated with patient survival 47 , 48 . In our study, a combination of DARTS technology and mass spectrometry-based proteomics, as well as SPR assay, revealed the direct binding of penfluridol to PFKL.…”
“…In the study by Zou et al (2014) , TRAF3IP2-AS1 expression was altered in gastric cancer cells after 125 I irradiation, providing a target for future drug development. AC099850.3 has been repeatedly extracted as a prognosis-related gene in the bioinformatics analysis of cancer, including squamous cell carcinoma of the tongue, hepatocellular carcinoma, and non-small cell lung cancer ( Hao Wu et al, 2020 ; Jia et al, 2020 ; Zheng et al, 2021a ; Junliang Zhou et al, 2021 ; Jiang et al, 2021 ; Wu et al, 2021 ; Xu et al, 2021 ; Zhang et al, 2021 ). The MIR193BHG motif can fine-tune cellular sterol/steroid biosynthesis by producing lincNORS to repress the expression of multiple pathway components ( Xue Wu et al, 2020 ).…”
Background: Long non-coding RNAs (lncRNAs) are key regulators of pancreatic cancer development and are involved in ferroptosis regulation. LncRNA transcript levels serve as a prognostic factor for pancreatic cancer. Therefore, identifying ferroptosis-related lncRNAs (FRLs) with prognostic value in pancreatic cancer is critical.Methods: In this study, FRLs were identified by combining The Cancer Genome Atlas (TCGA) and FerrDb databases. For training cohort, univariate Cox, Lasso, and multivariate Cox regression analyses were applied to identify prognosis FRLs and then construct a prognostic FRLs signature. Testing cohort and entire cohort were applied to validate the prognostic signature. Moreover, the nomogram was performed to predict prognosis at different clinicopathological stages and risk scores. A co-expression network with 76 lncRNA-mRNA targets was constructed.Results: Univariate Cox analysis was performed to analyze the prognostic value of 193 lncRNAs. Furthermore, the least absolute shrinkage and selection operator and the multivariate Cox analysis were used to assess the prognostic value of these ferroptosis-related lncRNAs. A prognostic risk model, of six lncRNAs, including LINC01705, AC068620.2, TRAF3IP2-AS1, AC092171.2, AC099850.3, and MIR193BHG was constructed. The Kaplan Meier (KM) and time-related receiver operating characteristic (ROC) curve analysis were performed to calculate overall survival and compare high- and low-risk groups. There was also a significant difference in survival time between the high-risk and low-risk groups for the testing cohort and the entire cohort, with AUCs of .723, .753, respectively. Combined with clinicopathological characteristics, the risk model was validated as a new independent prognostic factor for pancreatic adenocarcinoma through univariate and multivariate Cox regression. Moreover, a nomogram showed good prediction.Conclusion: The signature of six FRLs had significant prognostic value for pancreatic adenocarcinoma. They may be a promising therapeutic target in clinical practice.
“…The PGK1 gene encodes phosphoglycerate kinase enzyme, which is involved in a critical energy-producing process of glycolysis. Recently, PGK1 expression was reported as a part of a 7-gene signature and part of a 4-gene signature to predict the survival of breast cancer patients [ 23 , 24 ]. Furthermore, a higher expression of PGK1 was associated with poor prognosis in breast cancer, as it stimulated breast cancer progression and metastases [ 25 , 26 , 27 ].…”
We have previously found that sera from Crocodylus porosus contain anticancer agents and the treatment of MCF7 cells with this serum resulted in the differential expression of 51 genes. The purpose of this study was to use in silico analysis to identify genes that might be epigenetically modulated in cells treated with crocodile serum and to understand the role of potential genes as novel candidates with epigenetic therapeutic potential. The findings report five proto-oncogenes (TUBA1B, SLC2A1, PGK1, CCND1, and NCAPD2) and two tumor suppressor genes (RPLP2, RPL37) as novel therapeutic targets. Furthermore, we present a comprehensive overview of relevant studies on epigenetic regulation of these genes along with an insight into their clinical implications. Therefore, elucidating the molecules present in the serum and gut bacteria of reptiles such as crocodiles may offer insights into the role of these genes on longevity, health, disease, and life expectancy.
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