Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Kumar V Penmetsa"'
Autor:
Heather L Gardner, Sarah B Rippy, Misty D Bear, Kim L Cronin, Heather Heeb, Holly Burr, Claire M Cannon, Kumar V Penmetsa, Srikant Viswanadha, Swaroop Vakkalanka, Cheryl A London
Publikováno v:
PLoS ONE, Vol 13, Iss 4, p e0195357 (2018)
RV1001 is a novel, potent, and selective PI3Kδ inhibitor. The purpose of this study was to evaluate the safety and efficacy of RV1001 in canine Non-Hodgkin lymphoma (NHL).Inhibition of endogenous pAKT by RV1001 in primary canine NHL cells was determ
Externí odkaz:
https://doaj.org/article/2cde8c7101d8458aaeb72cfb3d0632c4
Autor:
Zui Pan, Srikant Viswanadha, Sangyong Choi, Liwu Fu, Yan Chang, Xiaoli Zhang, Kumar V. Penmetsa, Henry Tran, Chaochu Cui
Publikováno v:
Cancer Letters. 432:169-179
Esophageal cancer (EC) is the 6th leading cause of cancer mortality worldwide with poor prognosis, hence more effective chemotherapeutic drugs for this deadly disease are urgently needed. We previously reported that high expression of Orai1, a store-
Autor:
Philip A. Philip, Amro Aboukameel, Srikant Visvanadha, Kumar V. Penmetsa, Rachel E. Sexton, Ramzi M. Mohammad, Gabriel Mpilla, Asfar S. Azmi, Mohammad Najeeb Al-Hallak
Publikováno v:
Cancer Research. 80:234-234
Background: Dihydroorotate dehydrogenase (DHODH) is an enzyme which is critically involved in process of de novo pyrimidine biosynthesis. Therefore, it plays important roles in cell proliferation, mitosis and cellular metabolism. Importantly, overexp
Autor:
Mark Szlaczky, Maria Diab, Mohammed Najeeb Al-Hallak, Gabriel Mpilla, Srikant Viswanadha, Amro Aboukameel, Asfar S. Azmi, Steve Kim, Anteneh Tesfaye, Mandana Kamgar, Rachel E. Sexton, Philip A. Philip, Kumar V. Penmetsa, Husain Yar Khan, Ramzi M. Mohammad
Publikováno v:
Cancers, Vol 12, Iss 3, p 750 (2020)
Cancers
Volume 12
Issue 3
Cancers
Volume 12
Issue 3
Pancreatic ductal adenocarcinoma (PDAC) remains an unmet clinical problem in urgent need of newer molecularly driven treatment modalities. Calcium signals, particularly those associated with calcium release-activated calcium (CRAC) channels, are know
Publikováno v:
Molecular Cancer Therapeutics. 18:C045-C045
Background: Store-operated calcium entry (SOCE) through calcium release activated calcium (CRAC) channels contribute to calcium influx in non-excitable cells. Elevation of cytosolic calcium through SOCE mediates an array of cellular responses includi
Publikováno v:
Molecular Cancer Therapeutics. 18:C044-C044
Background: Interventions that promote differentiation of immature blasts have been shown to be a promising therapeutic strategy for the treatment of AML. Inhibition of dihydroorotate dehydrogenase (DHODH), a rate limiting enzyme in pyrimidine synthe
Autor:
Yan Chang, Chaochu Cui, Srikant Viswanadha, Xiaoli Zhang, Zui Pan, Kumar V. Penmetsa, Liwu Fu
Publikováno v:
The FASEB Journal. 32
Autor:
Shelley Orwick, Larry Beaver, Bridget Carmichael, Kumar V. Penmetsa, Erin Hertlein, John C. Byrd, Srikant Viswanadha, Jean Truxall, Ola A. Elgamal, Amy Lehman
Publikováno v:
Cancer Research. 78:1938-1938
Acute myeloid leukemia (AML) is the most prevalent adult leukemia characterized by genetic or mutational disruption of myeloid differentiation, growth arrest, and apoptosis. Standard “7 + 3” chemotherapy consisting of cytarabine in combination wi
Publikováno v:
Cancer Research. 78:1889-1889
Background: Multiple Myeloma (MM) accounts for approximately 2.1% of all cancer deaths with a 5-year median survival rate of 49.6%. Besides chemotherapy, treatment options include monoclonal antibodies, immunomodulatory agents, and proteasome inhibit
Autor:
Sarah B. Rippy, Claire M Cannon, Srikant Viswanadha, Kim L. Cronin, Heather L. Gardner, Cheryl A. London, Swaroop Vakkalanka, Kumar V. Penmetsa, Holly Burr, Heather Heeb, Misty D. Bear
Publikováno v:
PLoS ONE, Vol 13, Iss 4, p e0195357 (2018)
PLoS ONE
PLoS ONE
Background RV1001 is a novel, potent, and selective PI3Kδ inhibitor. The purpose of this study was to evaluate the safety and efficacy of RV1001 in canine Non-Hodgkin lymphoma (NHL). Methods and results Inhibition of endogenous pAKT by RV1001 in pri