S
Shan Naidu
Researcher at Louisiana State University
Publications - 30
Citations - 1175
Shan Naidu is an academic researcher from Louisiana State University. The author has contributed to research in topics: Ovarian cancer & Medicine. The author has an hindex of 13, co-authored 25 publications receiving 1042 citations. Previous affiliations of Shan Naidu include The Ohio State University Wexner Medical Center & University of Minnesota.
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Journal ArticleDOI
Pten in stromal fibroblasts suppresses mammary epithelial tumours
Anthony J. Trimboli,Carmen Z. Cantemir-Stone,Fu Li,Julie A. Wallace,Anand S. Merchant,Nicholas Creasap,John C. Thompson,Enrico Caserta,Hui Wang,Jean-Leon Chong,Shan Naidu,Guo Wei,Sudarshana M. Sharma,Julie A. Stephens,Soledad Fernandez,Metin N. Gurcan,Michael Weinstein,Sanford H. Barsky,Lisa D. Yee,Thomas J. Rosol,Paul C. Stromberg,Michael L. Robinson,Francois Pepin,Michael Hallett,Morag Park,Michael C. Ostrowski,Gustavo Leone,Gustavo Leone +27 more
TL;DR: The Pten–Ets2 axis is identified as a critical stroma-specific signalling pathway that suppresses mammary epithelial tumours and ameliorated disruption of the tumour microenvironment.
Journal ArticleDOI
Mouse development with a single E2F activator.
Shih-Yin Tsai,Rene Opavsky,Nidhi Sharma,Lizhao Wu,Lizhao Wu,Shan Naidu,Eric Nolan,Enrique Feria-Arias,Cynthia Timmers,Jana Opavska,Alain de Bruin,Jean Leon Chong,Prashant Trikha,Soledad Fernandez,Paul C. Stromberg,Thomas J. Rosol,Gustavo Leone +16 more
TL;DR: There is significant functional redundancy among activators and that the specific requirement for E2f3a during postnatal development is dictated by regulatory sequences governing its selective spatiotemporal expression and not by its intrinsic protein functions, providing a molecular basis for the observed specificity among E2F activators during development.
Journal ArticleDOI
Elevated STAT3 expression in ovarian cancer ascites promotes invasion and metastasis: a potential therapeutic target
Uksha Saini,Shan Naidu,Adam C. ElNaggar,Hemant K. Bid,John J. Wallbillich,Kristin Bixel,Chelsea Bolyard,Adrian A. Suarez,Balveen Kaur,Periannan Kuppusamy,John L. Hays,Paul J. Goodfellow,David E. Cohn,Karuppaiyah Selvendiran +13 more
TL;DR: The results show that STAT3 is necessary for ovarian tumor progression/metastasis and highlight the potential for targeting STAT3 by HO-3867 as a therapeutic strategy for ovarian cancer.
Journal ArticleDOI
Allele-specific tumor spectrum in pten knockin mice.
Hui Wang,Matt Karikomi,Matt Karikomi,Matt Karikomi,Shan Naidu,Shan Naidu,Shan Naidu,Ravi Rajmohan,Ravi Rajmohan,Ravi Rajmohan,Enrico Caserta,Enrico Caserta,Enrico Caserta,Hui-Zi Chen,Hui-Zi Chen,Hui-Zi Chen,Maysoon Rawahneh,Maysoon Rawahneh,Maysoon Rawahneh,Julie Moffitt,Julie Moffitt,Julie Moffitt,Julie A. Stephens,Soledad Fernandez,Michael Weinstein,Michael Weinstein,Michael Weinstein,Danxin Wang,Wolfgang Sadee,Krista M. D. La Perle,Paul C. Stromberg,Thomas J. Rosol,Charis Eng,Michael C. Ostrowski,Michael C. Ostrowski,Gustavo Leone,Gustavo Leone,Gustavo Leone +37 more
TL;DR: In this paper, the authors modeled three sentinel mutant alleles of PTEN identified in patients with Cowden syndrome and show that the nonsense Pten∆4-5 and missense PtenC124R and PtenG129E alleles lacking lipid phosphatase activity cause similar developmental abnormalities but distinct tumor spectra with varying severity and age of onset.
Journal ArticleDOI
HO-3867, a Safe STAT3 Inhibitor, Is Selectively Cytotoxic to Ovarian Cancer
Kellie S. Rath,Shan Naidu,Pushpa Lata,Hemant K. Bid,Brian K. Rivera,Georgia A. McCann,Brent J. Tierney,Adam C. ElNaggar,Veronica Bravo,Gustavo Leone,Peter J. Houghton,Kálmán Hideg,Periannan Kuppusamy,David E. Cohn,Karuppaiyah Selvendiran +14 more
TL;DR: The development of a novel class of bifunctional STAT3 inhibitors, based on conjugation of a diarylidenyl-piperidone backbone to an N-hydroxypyrroline (-NOH) group, which exhibits minimal toxicity against normal cells and good oral bioavailability and offers preclinical proof-of-concept for HO-3867 as a selective STAT3 inhibitor to treat ovarian cancer and other solid tumors where STAT3 is widely upregulated.