COCHRAN LABORATORY

'RSS


Search the Web:

Search Pubmed:

Tufts Seminars
TUSK knowledgebase
Tufts Directory

Search Tufts Directory:


Search Tufts:

 

Department of Development, Molecular and Cell Biology, Tufts University School of Medicine

136 Harrison Ave., Boston, Massachusetts, 02111, USA

Lab and Office: Jaharis Building, Room 708

Directions: Auto, MBTA, Foot, weather


Principal Investigator: Brent Cochran, Ph.D.,

Professor of Physiology

PHONE: (617) 636-0442 (office), (617) 636-6744(lab)

FAX: (617) 636-6745

EMAIL: COCHRAN@cochranlab.org


Coworkers:

Xue Zhang, Postdoctoral Associate

Shreya Kulkarni, Graduate Student

Sejuti Sengupta, Graduate Student

Surbhi Goel-Bhattacharya, Graduate Student


Former lab members

Jay Lee, MD/PhD Student (grad 2002)

Dae-Won Kim, Graduate Student (grad 2000)

Liza Konnikova, MD/PhD student

Matthew Kruger, Research Technician

Deepa Bhavsar, Postdoctoral Fellow

Maciej Kotecki, Postdoctoral Fellow

Joan Abrams Graduate Student(grad 2000)

Satoe Takahashi, Research Technician

Maureen Sherry, Graduate Student

Andrew Reeves, Graduate Student

Amy Simon, Assistant Prof. of Medicine


Research Interests:

My lab is broadly interested in how growth factors such as PDGF regulate cell growth. We are currently focused on developing new therapies for the adult brain tumor glioblastoma using cancer stem cells.. For several years we have been working on how the c-fos promoter is regulated. We discovered a growth factor inducible called SIF which turns out to be composed of STAT family transcription factors. We are currently interested in the role of STAT3 in cancer and in cancer stem cells in particular. We have been studying this primarily in the context of the glioblastoma brain cancer. The graphic at the top of the page shows cancer stem cells from a human glioblastoma growing as neurospheres on the left and stained with stem cell and neural markers. Another interest of the lab is the development of an annotated database of genes called MedStract in collaboration with a computational linguistics group at Brandeis. We are currently working on a DARPA project called "Communicating with Computers" to allow biologists to use natural language to discuss molecular pathways. Think of an enhanced Siri for the Cell. We have also pioneered the use of a human near haploid cell line for somatic cell genetics.
Click for a list of projects ongoing.


Useful Info

     

Projects

  • Role of STAT3 in gioblastoma stem cells
  • Identification of new therapeutic targets for GBM using RNAi and CRISPR/div>
  • Mechanism of activation of Stats by PDGF
  • Regulation of c-fos by the Jak/Stat pathway
  • Cell cycle regulation of growth factor signalling
  • Development of human haploid cells as a genetic system.
  • Development of a natural language computer dialog system for discussing biological pathways

Selected Publications:

Sherry-Lynes, MM, Segupta, S, Kulkarni, S, Cochran BH. 2016. Regulation of the JMJD3 (KDM6B) histone demethylase in glioblastoma stem cells by STAT3. PLOS ONE 12(4): e0174775 Abstract , pdf

Carette JE, Guimaraes CP, Varadarajan M,  Park AS, Wuethrich I, Godarova I, Kotecki M,  Cochran BH, Spooner E, . Ploegh HL, and Brummelkamp TR. 2009. Haploid Genetic Screens in Human Cells Identify Host Factors Used by Pathogens. Science 326:1231-5. Abstract , pdf

Sherry MM, Reeves A, Wu JK, Cochran BH. 2009. STAT3 is required for proliferation and maintenance of multipotency in glioblastoma stem cells. Stem Cells, 27:2383 - 2392. abstract, pdf

Konnikova L, Simeone MC, Kruger MM, Kotecki M, Cochran BH. 2005. Signal transducer and activator of transcription 3 (STAT3) regulates human telomerase reverse transcriptase (hTERT) expression in human cancer and primary cells. Cancer Res. 65(15):6516-20. Abstract

Konnikova L, Kotecki M, Kruger MM, Cochran BH. 2003. Knockdown of STAT3 expression by RNAi induces apoptosis in astrocytoma cells. BMC Cancer 2:23. free full text, pdf

Simon AR, Takahashi S, Severgnini M, Fanburg BL, Cochran BH. 2002. Role of the JAK-STAT pathway in PDGF-stimulated proliferation of human airway smooth muscle cells. Am J Physiol Lung Cell Mol Physiol Jun;282(6):L1296-304. abstract, full text

Kim, D.-W. and B.H. Cochran. 2001. Jak2 activates tfii-i and regulates its interaction with extracellular signal-regulated kinase. Mol Cell Biol. 2001 May 15;21(10):3387-97. abstract, pdf

Simon AR, Vikis HG, Stewart S, Fanburg BL, Cochran BH, Guan KL. 2000. Regulation of STAT3 by direct binding to the rac1 GTPase. Science 2000 Oct 6;290(5489):144-7. Abstract, pdf

Kim, D.-W. and B.H. Cochran. 2000. ERK binds to TFII-I and regulates its activation of the c-fos promoter. Mol. Cell Biol. 20(4):1140-8. abstract, pdf

Kotecki, M., P. S. Reddy, and B. H. Cochran. 1999. Isolation and characterization of a near-haploid human cell line. Exp Cell Res, Nov 1;252(2):273-80. abstract, pdf

Grammatikakis, N., Lin, J.-H., Grammatikakis, A., Tsichlis, P. N. and Cochran, B. H. (1999). p50cdc37 acting in concert with Hsp90 is required for Raf-1 function. Mol. Cell Biol., 19, 1661-72. abstract, pdf

Kim, D.-W., Cheriyath, V., Roy, A. L. and Cochran, B. H. (1998). TFII-I enhances activation of the c-fos promoter through interactions with upstream elements. Mol. Cell. Biol. 18, 3310-3320.abstract, pdf

Simon, A, Rai, U., Fanburg, B. Cochran BH. 1998. Activation of the JAK/STAT pathway by reactive oxygen species. Am. J. of Physiology,44, C1640-C1652. abstract, (Download full text PDF file)

Hayes TE, Kitchen AM, Cochran BH. 1987. Inducible binding of a factor to the c-fos regulatory region. Proc. Natl. Acad. Sci. (USA) 84: 1272-1276.

Sengupta P, Cochran BH. 1991. MATalpha1 can mediate gene activation by a-mating factor. Genes and Dev. 5: 1924-1934.

Meyer, D. J., Campbell, G., Cochran, B. H., Argetsinger, L., Larner, A. C., Finbloom, D. S., Carter-Su, C. and Schwartz, J. 1993. Growth hormone induces a DNA-binding factor related to the interferon-stimulated 91-kDa transcription factor. J. Biol. Chem. 269, 4701-4704.

Abstracts


Physiology Dept.**** Health Science Campus


visits since January 24,2017