Related Experiment Video
Updated: Aug 13, 2026

Synchronous Triplanar Reconstruction Integrated with Color Doppler Mapping for Precise and Rapid Localization of Thyroid Lesions
Published on: February 9, 2024
AcSDKP: a new potential marker of malignancy of the thyroid gland
Michal Kusinski1, Joanna Wdzieczak-Bakala, Jian-Miao Liu
1General and Endocrine Surgery Department, Medical University of Lodz, Lodz, Poland. rmk@toya.net.pl
Background And Aims:
The tetrapeptide Acetyl-Ser-Asp-Lys-Pro (AcSDKP) a physiologic inhibitor of stem-cell proliferation is also known for it's strong angiogenic activity. It has been shown that blood levels of this peptide are increased in some hematological malignancies. However, no data on the concentration of AcSDKP present in solid tumor tissue are available. The aim of our study was to measure tissue concentration of AcSDKP in benign and malignant lesions of the thyroid gland.
Patients And Methods:
We assessed AcSDKP level in thyroid tissue specimens using enzyme immunoassay kit. The specimens were taken intraoperatively from 20 patients (17 women and 3 men aged 21-68 years): 10 patients with benign nodular goiter and 10 patients with papillary carcinoma of the thyroid gland.
Results:
The obtained results show that tissue concentration of AcSDKP in malignant thyroid tumors is five times higher when compared to benign lessions.
Conclusion:
We conclude that AcSDKP may play a role in the development of the thyroid gland lesions. However, the further investigations concerning the tetrapeptide concentration in other thyroid malignancies, toxic nodular, and Grave's goiter are required to conclude on the eventual use of AcSDKP as a marker of malignancy.
Related Concept Videos
Graves Disease II: Pathophysiology
M-Cdk Drives Transition Into Mitosis
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
