2019
DOI: 10.1016/j.prp.2019.01.003
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Contribution and prognostic value of TSGA10 gene expression in patients with acute myeloid leukemia (AML)

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Cited by 10 publications
(10 citation statements)
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“…The negative relationship between expression of TSGA10 and HIF-α subunits was also verified in both cervical and breast cancer [32]. In acute myeloid leukemia, the interaction between TSGA10 and HIF1-α leads to a decrease in VEGF secretion [29]. This suggests there may be a feedback loop among HIF1-α, miR-10b-3p and TSGA10 in ESCC cells, which deserves further exploration.…”
Section: Discussionmentioning
confidence: 97%
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“…The negative relationship between expression of TSGA10 and HIF-α subunits was also verified in both cervical and breast cancer [32]. In acute myeloid leukemia, the interaction between TSGA10 and HIF1-α leads to a decrease in VEGF secretion [29]. This suggests there may be a feedback loop among HIF1-α, miR-10b-3p and TSGA10 in ESCC cells, which deserves further exploration.…”
Section: Discussionmentioning
confidence: 97%
“…TSGA10 is initially characterized as a testis-specific protein and tumor-associated antigen that facilitates angiogenesis and metastasis in various cancers [27]. The prognostic value of TSGA10 is also identified in acute myeloid leukemia and transitional cell carcinoma of the bladder [28, 29]. In ESCC, TSGA10 down-regulation is shown to be associated with a progressive clinical stage, and in vivo assays suggest TSGA10 knockdown significantly accelerates tumor growth and leads to larger tumor volumes [30].…”
Section: Discussionmentioning
confidence: 99%
“…Reverse transcription for 500 ng of the total RNA extracted from all samples was performed using both random hexamer and oligo‐dT primers. The sense and antisense primers for genes of target and reference were designed using robust oligo primer design software (synthesized by the Bioneer Company) . The sequences of the oligonucleotide primers for qPCR analysis are listed in Table .…”
Section: Methodsmentioning
confidence: 99%
“…Total RNA was extracted from the testis tissue samples both from patients and the control group using Trizol reagent (Invitrogen, Carldbad, CA, USA) in accordance with the manufacturer's instructions. 16 The quality and quantity of each sample were assessed using a NanoDropND-2000 Spectrophotometer (Thermo Fisher Scientific, Wilmington, DE, USA), and their integrity was confirmed by electrophoresis on 1% agarose gel (Ultra-Pure TM Agarose; Invitrogen), and then they underwent Gel Red RNA staining, followed by detection under an ultraviolet light. The high-quality RNA samples with no degradation were stored at −80 C and the first-strand cDNA was synthesized using a cDNA synthesis kit (Fermentas, Waltham, MA, USA).…”
Section: Quantitative Real-time Polymerase Chain Reaction (Qpcr) Anmentioning
confidence: 99%
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