Determination of the effects of Traf2 and Nck-interacting protein kinase (TNIK) inhibitor on PI3K/Akt/mTOR signaling in canine lipid-rich carcinoma cells


Baykal A., Güney G., Deveci A., Turna Ö.

6th International Congress on Advances in Bioscience and Biotechnology, Aksaray, Türkiye, 25 - 29 Temmuz 2022, ss.54-60, (Tam Metin Bildiri)

  • Yayın Türü: Bildiri / Tam Metin Bildiri
  • Basıldığı Şehir: Aksaray
  • Basıldığı Ülke: Türkiye
  • Sayfa Sayıları: ss.54-60
  • İstanbul Üniversitesi-Cerrahpaşa Adresli: Evet

Özet

Mammary gland tumors have the highest incidence among dogs. Lipid-rich carcinoma is very rare histological types of mammary tumor. However, it is generally observed in young female dogs and the success of current treatment option is limited. Therefore, innovative approaches are required for the treatment of canine mammary tumors. Traf2 and Nck-Interacting (TNIK) is a member of the mitogenactivated serine/threonine protein kinase family regulates Wnt signaling pathway. Additionally, the phosphatidylinositol-3-kinase (PI3K)/Akt and mammalian targeting of rapamycin (mTOR) signaling pathways is crucial for many aspects of cancer cell growth. Therefore, we aimed to determine the effect of NCB-0684 as a TNIK inhibitor on PI3K/Akt/mTOR signaling in canine lipid-rich carcinoma cells via determination of Akt and mTOR mRNA levels with RT-PCR analysis. Our findings demonstrated that NCB0684 inhibited Akt and mTOR gene expression levels at higher concentration. However, the effectiveness of TNIK inhibitor is changed dependently its concentration. Thus, our results claim that NCB-0684 could suppress PI3K/Akt/mTOR signaling. However, further investigations need to clarify the inhibitory activity of TNIK inhibitor on PI3K/Akt/mTOR signaling in canine mammary tumors.