P
Prabhu Thirusangu
Researcher at Mayo Clinic
Publications - 36
Citations - 668
Prabhu Thirusangu is an academic researcher from Mayo Clinic. The author has contributed to research in topics: Cancer cell & In vivo. The author has an hindex of 13, co-authored 29 publications receiving 441 citations. Previous affiliations of Prabhu Thirusangu include Kuvempu University.
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Journal ArticleDOI
Synthesis and tumor inhibitory activity of novel coumarin analogs targeting angiogenesis and apoptosis.
B.R. Vijay Avin,Prabhu Thirusangu,V. Lakshmi Ranganatha,Aiyesha Firdouse,B.T. Prabhakar,Shaukath Ara Khanum +5 more
TL;DR: In vivo antitumor effect of compound 5c against murine EAC and solid DL tumor model system was evident by the extended survivality and the tumor inhibitory mechanism of compounds 5c was due to the antiangiogenesis and promotion of apoptosis.
Journal ArticleDOI
Repurposing quinacrine for treatment-refractory cancer.
Derek B. Oien,Christopher L. Pathoulas,Upasana Ray,Prabhu Thirusangu,Eleftheria Kalogera,Viji Shridhar +5 more
TL;DR: Repurposing quinacrine as an anticancer agent appears to be a promising strategy based on its ability to target multiple pathways, its selectivity against cancer cells, and the synergistic cytotoxicity when combined with other anticancer agents with limited side effects and good tolerability profile.
Journal ArticleDOI
BP-1T, an antiangiogenic benzophenone-thiazole pharmacophore, counteracts HIF-1 signalling through p53/MDM2-mediated HIF-1α proteasomal degradation
Prabhu Thirusangu,V. Vigneshwaran,T. Prashanth,B.R. Vijay Avin,B.R. Vijay Avin,Vikas H. Malojirao,H. Rakesh,Shaukath Ara Khanum,Riaz Mahmood,B.T. Prabhakar +9 more
TL;DR: It is concluded that BP-1T acts on HIF-1α degradation through p53/MDM2 proteasome pathway, eventually leading to abolition of migration and invasion in solid tumour.
Journal ArticleDOI
Synthesis, angiopreventive activity, and in vivo tumor inhibition of novel benzophenone-benzimidazole analogs.
V. Lakshmi Ranganatha,B.R. Vijay Avin,Prabhu Thirusangu,T. Prashanth,B.T. Prabhakar,Shaukath Ara Khanum +5 more
TL;DR: Analyzing the structure-activity relationship, it is found that an increase in the number of methyl groups in addition to methoxy substitution at the para position of the benzoyl ring in compound 8n resulted in higher potency compared to 8f.
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Synthesis of coumarin analogs appended with quinoline and thiazole moiety and their apoptogenic role against murine ascitic carcinoma.
T. Prashanth,B.R. Vijay Avin,Prabhu Thirusangu,V. Lakshmi Ranganatha,B.T. Prabhakar,J. N. Narendra Sharath Chandra,Shaukath Ara Khanum +6 more
TL;DR: Experimental data showed that compound 13f induces the apoptotic cell death by activating apoptotic factors such as caspase-8 &-3, CAD, Cleaved PARP, γ-H2AX and by degrading genomic DNA of cancer cells and thereby decreasing the ascitic tumour development in mice.