Sunil R Hingorani

Summary

Affiliation: University of Pennsylvania
Country: USA

Publications

  1. ncbi Trp53R172H and KrasG12D cooperate to promote chromosomal instability and widely metastatic pancreatic ductal adenocarcinoma in mice
    Sunil R Hingorani
    Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA
    Cancer Cell 7:469-83. 2005
  2. ncbi Ras redux: rethinking how and where Ras acts
    Sunil R Hingorani
    Abramson Family Cancer Research Institute, Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA
    Curr Opin Genet Dev 13:6-13. 2003
  3. ncbi N-cadherin and keratinocyte growth factor receptor mediate the functional interplay between Ki-RASG12V and p53V143A in promoting pancreatic cell migration, invasion, and tissue architecture disruption
    Therese B Deramaudt
    Gastroenterology Division, University of Pennsylvania, 415 Curie Boulevard, Philadelphia, PA 19104 2144, USA
    Mol Cell Biol 26:4185-200. 2006
  4. ncbi In search of an early warning system for pancreatic cancer
    Sunil R Hingorani
    Departments of Cancer Biology and Medicine, Abromson Family Cancer Research Institute, University of Pennsylvania Medical Center, Philadelphia, PA 19104, USA
    Cancer Biol Ther 2:84-6. 2003
  5. ncbi Targeting oncogene dependence and resistance
    Sunil R Hingorani
    Abramson Family Cancer Research Institute, Abramson Cancer Center of the University of Pennsylvania School of Medicine, Department of Medicine, Philadelphia 19104, USA
    Cancer Cell 3:414-7. 2003
  6. ncbi New pathways to pancreatic cancer
    Sunil R Hingorani
    Department of Cancer Biology, Abramson Family Cancer Research Institute, University of Pennsylvania Medical Center, 421 Curie Blvd, 521 BRB II/III, Philadelphia, Pennsylvania 19104, USA
    Cancer Biol Ther 3:170-2. 2004
  7. ncbi Endogenous oncogenic K-ras(G12D) stimulates proliferation and widespread neoplastic and developmental defects
    David A Tuveson
    Abramson Family Cancer Research Institute, Abramson Cancer Center and Department of Medicine, University of Pennsylvania, Philadelphia, PA 19104 USA
    Cancer Cell 5:375-87. 2004
  8. ncbi Dynamics of the immune reaction to pancreatic cancer from inception to invasion
    CAROLYN E CLARK
    Abramson Family Cancer Research Institute, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA
    Cancer Res 67:9518-27. 2007
  9. ncbi Preinvasive and invasive ductal pancreatic cancer and its early detection in the mouse
    Sunil R Hingorani
    Department of Medicine, Abramson Family Cancer Research Institute, Abramson Center at the University of Pennsylvania, Philadelphia, PA 19104, USA
    Cancer Cell 4:437-50. 2003
  10. ncbi ATP citrate lyase inhibition can suppress tumor cell growth
    Georgia Hatzivassiliou
    Department of Cancer Biology, Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, PA 19104, USA
    Cancer Cell 8:311-21. 2005

Detail Information

Publications18

  1. ncbi Trp53R172H and KrasG12D cooperate to promote chromosomal instability and widely metastatic pancreatic ductal adenocarcinoma in mice
    Sunil R Hingorani
    Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA
    Cancer Cell 7:469-83. 2005
    ..These findings have clear implications for understanding mechanisms of disease pathogenesis, and for the development of detection and targeted treatment strategies...
  2. ncbi Ras redux: rethinking how and where Ras acts
    Sunil R Hingorani
    Abramson Family Cancer Research Institute, Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA
    Curr Opin Genet Dev 13:6-13. 2003
    ..Recent findings have provided new and unexpected insights into the predominant pathways Ras employs to transform human cells and the subcellular platforms from which it can act...
  3. ncbi N-cadherin and keratinocyte growth factor receptor mediate the functional interplay between Ki-RASG12V and p53V143A in promoting pancreatic cell migration, invasion, and tissue architecture disruption
    Therese B Deramaudt
    Gastroenterology Division, University of Pennsylvania, 415 Curie Boulevard, Philadelphia, PA 19104 2144, USA
    Mol Cell Biol 26:4185-200. 2006
    ..Thus, we are able to define molecules that in part are directly affected by Ki-RAS and p53 during pancreatic ductal carcinogenesis, and this provides a platform for potential new molecularly based therapeutic interventions...
  4. ncbi In search of an early warning system for pancreatic cancer
    Sunil R Hingorani
    Departments of Cancer Biology and Medicine, Abromson Family Cancer Research Institute, University of Pennsylvania Medical Center, Philadelphia, PA 19104, USA
    Cancer Biol Ther 2:84-6. 2003
  5. ncbi Targeting oncogene dependence and resistance
    Sunil R Hingorani
    Abramson Family Cancer Research Institute, Abramson Cancer Center of the University of Pennsylvania School of Medicine, Department of Medicine, Philadelphia 19104, USA
    Cancer Cell 3:414-7. 2003
    ..Recent findings reveal several mechanisms of resistance and suggest ways to overcome them...
  6. ncbi New pathways to pancreatic cancer
    Sunil R Hingorani
    Department of Cancer Biology, Abramson Family Cancer Research Institute, University of Pennsylvania Medical Center, 421 Curie Blvd, 521 BRB II/III, Philadelphia, Pennsylvania 19104, USA
    Cancer Biol Ther 3:170-2. 2004
  7. ncbi Endogenous oncogenic K-ras(G12D) stimulates proliferation and widespread neoplastic and developmental defects
    David A Tuveson
    Abramson Family Cancer Research Institute, Abramson Cancer Center and Department of Medicine, University of Pennsylvania, Philadelphia, PA 19104 USA
    Cancer Cell 5:375-87. 2004
    ..Our results suggest that endogenous oncogenic ras is sufficient to initiate transformation by stimulating proliferation, while further genetic lesions may be necessary for progression to frank malignancy...
  8. ncbi Dynamics of the immune reaction to pancreatic cancer from inception to invasion
    CAROLYN E CLARK
    Abramson Family Cancer Research Institute, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA
    Cancer Res 67:9518-27. 2007
    ..Efforts to test potent inhibitors of MDSC, tumor-associated macrophages, and Treg, particularly early in the disease represent important next steps for developing novel immunotherapy of cancer...
  9. ncbi Preinvasive and invasive ductal pancreatic cancer and its early detection in the mouse
    Sunil R Hingorani
    Department of Medicine, Abramson Family Cancer Research Institute, Abramson Center at the University of Pennsylvania, Philadelphia, PA 19104, USA
    Cancer Cell 4:437-50. 2003
    ..Finally, mice with PanINs have an identifiable serum proteomic signature, suggesting a means of detecting the preinvasive state in patients...
  10. ncbi ATP citrate lyase inhibition can suppress tumor cell growth
    Georgia Hatzivassiliou
    Department of Cancer Biology, Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, PA 19104, USA
    Cancer Cell 8:311-21. 2005
    ..ACL inhibition by RNAi or the chemical inhibitor SB-204990 limits in vitro proliferation and survival of tumor cells displaying aerobic glycolysis. The same treatments also reduce in vivo tumor growth and induce differentiation...
  11. ncbi Detecting and diagnosing ampullary neoplasms
    Li-Fu Wang
    Departments of Cancer Biology and Medicine, Abramson Family Cancer Research Institute, The Abramson Cancer Center at the University of Pennsylvania Medical Center, Philadelphia, Pennsylvania 19104, USA
    Cancer Biol Ther 3:657-9. 2004
  12. ncbi A phase I trial of the oral, multikinase inhibitor sorafenib in combination with carboplatin and paclitaxel
    Keith T Flaherty
    The Abramson Cancer Center of the University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA
    Clin Cancer Res 14:4836-42. 2008
    ..Pharmacokinetic analyses were done for sorafenib on days 2 and 19 of cycle 1 and for paclitaxel on day 1 of cycles 1 and 2. Pretreatment tumor samples from 17 melanoma patients were analyzed for BRAF mutations...
  13. ncbi Suppression of BRAF(V599E) in human melanoma abrogates transformation
    Sunil R Hingorani
    Abramson Family Cancer Research Institute at the University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA
    Cancer Res 63:5198-202. 2003
    ..Thus, when present, BRAF(V599E) appears to be essential for melanoma cell viability and transformation and, therefore, represents an attractive therapeutic target in the majority of melanomas that harbor the mutation...
  14. ncbi Kras(G12D) and Smad4/Dpc4 haploinsufficiency cooperate to induce mucinous cystic neoplasms and invasive adenocarcinoma of the pancreas
    Kamel Izeradjene
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA
    Cancer Cell 11:229-43. 2007
    ..Our findings suggest that the sequence, as well as the context, in which these critical mutations are acquired helps determine the ensuing pathology...
  15. ncbi The RON receptor tyrosine kinase mediates oncogenic phenotypes in pancreatic cancer cells and is increasingly expressed during pancreatic cancer progression
    Ryan M Thomas
    Division of Surgical Oncology, Department of Surgery, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA
    Cancer Res 67:6075-82. 2007
    ..Taken together, these findings suggest that RON receptor signaling may contribute to pancreatic carcinogenesis, and that further investigation is warranted to assess the potential of RON-directed therapies in this deadly disease...
  16. ncbi Location, location, location: precursors and prognoses for pancreatic cancer
    Sunil R Hingorani
    Gastroenterology 133:345-50. 2007
  17. ncbi Targets, trials, and travails in pancreas cancer
    Kamel Izeradjene
    Clinical Research and Public Health Sciences Divisions, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109 1024, USA
    J Natl Compr Canc Netw 5:1042-53. 2007
    ..New potential targets in the treatment of this formidable disease are suggested based on recent findings...
  18. ncbi EGCG inhibits growth, invasion, angiogenesis and metastasis of pancreatic cancer
    Sharmila Shankar
    Department of Biochemistry, University of Texas Health Science Center at Tyler, Tyler, Texas 75703, USA
    Front Biosci 13:440-52. 2008
    ..Overall, our data suggest that EGCG inhibits pancreatic cancer growth, invasion, metastasis and angiogenesis, and thus could be used for the management of pancreatic cancer prevention and treatment...