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Thymosin-alpha-1

Thymalfasin, Zadaxin, Thymosin α1

Quick Stats
Studies 759
Trials 63
Score 1
2012 pubmed 13 citations

Plasma thymosin-α1 level as a potential biomarker in urothelial and renal cell carcinoma.

Jou. Yeong-Chin YC; Tsai. Yuh-Shyan YS; Hsieh. Hsiao-Yen HY; Chen. Syue-Yi SY; Tsai. Hsin-Tzu HT; Chen. Ko-Jung KJ; Wang. Shan-Tair ST; Shiau. Ai-Li AL; Wu. Chao-Liang CL; Tzai. Tzong-Shin TS

Key Findings

  • TA1 levels were significantly lower in renal cell carcinoma patients compared to bladder cancer and benign cases
  • TA1 levels dropped as cancer stage increased in both bladder and kidney cancers
  • Low TA1 predicted shorter progression‑free and disease‑specific survival in bladder cancer

Practical Outcomes

  • For most biohackers this research isn’t directly useful because it’s about a diagnostic marker, not a supplement or therapy. It may be of interest if you or a loved one are being evaluated for these cancers, but it doesn’t provide actionable steps for healthy individuals looking to boost longevity or performance.

Summary

The study measured a protein called thymosin‑alpha‑1 (TA1) in the blood of people with kidney or bladder cancers and found that lower levels were linked to more advanced disease and worse outcomes, especially in bladder cancer, but it doesn’t tell you how to use TA1 for health improvement.

Abstract

To determine the plasma levels of thymosin-α1 (TA1) and prothymosin-α (PTMA) proteins in renal cell carcinoma (RCC) or urothelial carcinoma (UC) patients, and explore the potential of these 2 molecules as biomarkers. Blood samples were taken from 50 consecutive patients with RCC, 97 with UC, and 55 with benign urologic diseases before surgery. Their clinical characteristics were obtained from medical record review. Plasma TA1 and PTMA levels were measured using enzyme-linked immunosorbent assay and their correlation with tumor grade, pathologic stage, and survival were explored. Plasma TA1 levels were significantly lower in RCC patients than in UC or benign patients, particularly in UC of the renal pelvis patients (P < 0.0001). Plasma PTMA levels were also significantly lower in UC patients compared with RCC patients and benign patients (P < 0.05). Plasma TA1 levels inversely correlated with pathologic stage both in bladder cancer and RCC patients (P = 0.03 and 0.02, respectively). Both plasma TA1 and PTMA did not correlate with tumor grade. Plasma TA1 was a prognostic indicator for progression-free and disease-specific overall survival in bladder cancer patients (P = 0.008 and 0.04, respectively). Plasma TA1 level may be a biomarker for differentiating between UC and RCC. It may also be a prognostic factor for disease progression and disease-specific survival in bladder cancer patients. These findings warrant more studies for validation.

Study Information

Provider

pubmed

Year

2012

Date

2012-05-19T00:00:00.000Z

DOI

10.1016/j.urolonc.2012.03.011

Citations

13

References

27