BMP Receptor 1A Juvenile Polyposis Dayna Neo 3/21/13 Biol 445 001.

Slides:



Advertisements
Similar presentations
What is Li-Fraumeni syndrome?
Advertisements

Mechanisms and Epidemiology of Colon Cancer
BMP Receptor 1 : Juvenile Polyposis (Colon Cancer) Cecily Johnson Biology 169 March 24, 2005.
A tumor suppressor gene
Peutz-Jeghers Syndrome: LBK1/STK11 By Matt Wheeler.
ZAFIA ANKLESARIA Role of BMPR1A in Juvenile Polyposis Syndrome Biology 169.
SMAD4/DPC4: A Tumor Suppressor James Brooks March 23 rd, 2006.
LKB1 and Peutz-Jeghers Syndrome Josh Lawrimore. Gene Specifics.
Transforming Growth Factor β Receptor Type II Tina Morris
BMP receptor1a Amit Patel Estimated US Cancer Deaths* ONS=Other nervous system. Source: American Cancer Society, Men 295,280 Women 275,000.
BioSci 145A lecture 18 page 1 © copyright Bruce Blumberg All rights reserved BioSci 145A Lecture 18 - Oncogenes and Cancer Topics we will cover today.
NF2 = gene Merlin = protein…a.k.a. schwannomin Tumor Suppressor Tumor suppressive ability comes from partial inhibition of Ras/Rac signaling (phosphorylates.
BRCA2 Blue: Rad51; Green: BRCA2
Transforming Growth Factor-Beta Receptor 2 TGF-β receptor 2
Colon cancer is the second leading cause of cancer deaths in the U.S. Polyps, the first stage In tumor development
Colon cancer is the second leading cause of cancer deaths in the U.S. Polyps, the first stage In tumor development
RET Proto- Oncogene in The Development of Thyroid Cancer: Multiple Endocrine Neoplasia Type 2 Courtney Brooks.
In vivo animal model studies in biological science 1.Cancer 2. Neuroscience 1.Cancer research 2. Neuroscience.
Tumor Supressor Gene Non-functional TSG Mutations increasing risk of cancer “Loss of function” mutation Proto-oncogene Oncogene (Hyperactive or unregulated.
Building a Model of Tumorigenesis: A small group activity for a Cancer Biology/Cell Biology course L. K. Wright Supplemental File : Multistep Tumorigenesis.
Malignant Melanoma and CDKN2A
HIC1 attenuates Wnt signaling by recruitment TCF-4 and β-catenin to the nuclear bodies EMBO Journal (2006)
Advanced Cancer Topics Journal Review 4/16/2009 AD.
Prof. Janusz Limon, MD, PhD
Familial Cancer. General Principles Mutations inherited through germ cells contribute to a minority of tumours Two hits usually needed germline/somatic.
TGF-β Receptor I/ALK5: An Attractive Therapeutic Target in Tumor Development By Jake Bridgers.
Β-Catenin, Cancer, and G Proteins Not Just for Frizzleds Anymore Ming Yang et al. PNAS Maria Domenica Castellone et al. Science
Computational biology of cancer cell pathways Modelling of cancer cell function and response to therapy.
BRCA1: Tumor Suppression and Breast Cancer A breast cancer cell dividing.
Problem 1 James is the only person in his kindred affected by DMD. He has one unaffected brother, Joe. DNA analysis show that James has a deletion in the.
P57, Tumorigenesis, and Beckwith-Wiedemann Syndrome Ashley Albright.
Smad4 in Colon & Pancreatic Cancers
FGFR3 and Bladder Cancer Amy Fair March 29, 2005 Biol 169.
BMPR1A Bone Morphogenetic Protein Receptor 1 A (Juvenile Polyposis & Colon Cancer) Hallie Wieters.
Ishita Das
TSC1 and Facial Angiofibromas
BMP receptor1A Presented by Jena Buchan
Types of Genes Associated with Cancer
TSC1/Hamartin and Facial Angiofibromas Biology 169 Ann Hau.
PTEN (Cowden Syndrome) /.../ sld083.htm.
PTEN (Phosphatase and Tensin Homolog) a.k.a. MMAC1, TEP1 Raymond Stadiem.
Chapter 11 Cancer Genetics. Cell responses to environmental signals.
Cowden’s Disease and PTEN. Cowden’s Disease (CD)  A rare autosomal dominant disease similar to Lehrmitte-Duclos Disease (LDD) and Bannayan-Zonana Syndrome.
Rhythmic Control of the ARF-MDM2 Pathway by ATF4 Underlies Circadian Accumulation of p53 in Malignant Cells Michiko Horiguchi1Michiko Horiguchi1,2,
Kate Bradford BIOL 445 March 5, 2009
Peutz-Jeghers Syndrome and LKB1/STK11
The Role of SMAD4 (DPC4) in Cancer
Bone Morphogenetic Protein Receptor 1A (BMPR1A) and Juvenile Polyposis Syndrome Cara Davidson March 18, 2004.
and multiple endocrine neoplasia type 2 (MEN2)
TSC1 in Facial Angiofibromas
TSC2 GENE ENCODES FOR TUBERIN
Genetics of Cancer.
Colorectal cancer : Three pathways
The promise of cancer genetics
PTEN (a.k.a. MMAC1 and TEP1) and Cowden’s Disease
Nat. Rev. Endocrinol. doi: /nrendo
Dan Gordon  Gastroenterology  Volume 114, Issue 4, (April 1998)
Notch1 and its role in pre-T-cell acute lymphoblastic leukemia (T-ALL)
Mutation Screening in Juvenile Polyposis Syndrome
Extracellular Regulation of Apoptosis
The Role of MSH2 in Hereditary Non-Polyposis Colon Cancer
PTEN Tumor Suppressor Extraordinaire
Volume 134, Issue 5, Pages e3 (May 2008)
PTEN Tumor Suppressor and Cancer
The promise of cancer genetics
BMP Receptor 1a and Juvenile Polyposis Syndrome
Volume 133, Issue 3, Pages (September 2007)
Multifunctional Tumor Suppressor
Canonical gliomagenesis mediators EGFR, P53, and retinoblastoma protein (RB1) are important for cancer signaling. Canonical gliomagenesis mediators EGFR,
Neoplasia lecture 7 Dr Heyam Awad FRCPath.
Presentation transcript:

BMP Receptor 1A Juvenile Polyposis Dayna Neo 3/21/13 Biol

Juvenile Polyposis is a rare autosomal dominant syndrome that increases your risk of intestinal tract cancer Humpath.com Juvenile Polyposis Daniel Calva, MD and James Howe, MD.

BMPR1A is a receptor serine/threonine kinase that phosphorylates SMAD transcription factors Hardwick, James C et al

BMPR1A is a tumor suppressor!!!!

BMP pathway inhibits proliferation by inhibiting the Wnt pathway BMP Pathway PTEN Wnt Cell Proliferation COX-2 expression EGF receptor

Two-hit hypothesis and loss of heterozygosity leads to Juvenile Polyposis Deletions, insertions, and missense/nonsense mutations  abnormally short, nonfunctional protein No mutations observed in transmembrane domain >90% penetrance Jyh-Cherng Yu and Chen Yang Shen

Individuals with juvenile polyposis have mutations in their BMPR1A James R. Howe et. al DE B S

Arrows represent bands corresponding to BMP1A mutations James R. Howe et. al Individual 12 will get JP D B E S

BMPR1A is present at the base of each intestinal crypt Hardwick, James C et al Crypt Villus

BMPR1A -/- lack the mesoderm layer during gastrulation Mishina Y et al

Treatments include polypectomy, prophylactic colectomy, and restorative proctocolectomy A subject of current investigation involves cycloxygenase inhibitors Cleavelandclinic.org

References Bessa, P.C et al, Bone morphogenetic proteins in tissue engineering: the road from the laboratory to the clinic, part I(basic concepts). Journal of Tissue Engineering and Regenerative Medicine 2008:2:1-13 Hardwick, James C et al, Bone morphogenic protein signaling in colorectal cancer. Nature Reviews: Cancer 2008: 8: Children’s Hospital Boston, JR Howe, et. al, Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis. Nature JR Howe, et.al, The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations. J Med Genet 2004, 41: Juvenile Polyposis : (SMAD4) Sequencing and Deletion/Duplication, (BMPR1A) Sequencing and Deletion/Duplication Kurland JE, et al, Cyclooxygenase-2 expression in polyps from a patient with juvenile polyposis syndrome with mutant BMPR1A. J Pediatr Gastroenterol Nutr. 2007, Mar;44(3): Lodewijk AA Brosens et, al. Juvenile polyposis syndrome. World Journal of Gastroenterology. Mishina, Y. et al, Bmpr encodes a type I bone morphogenetic protein receptor that is essential for gastrulation during mouse embryogenesis. Genes, Dev Genes & Development. Tian, Qiang et al, Bridging the BMP and Wnt Pathways by PI3 Kinase/Akt and Landes Bioscience. Cell Cycle 4: : February 2005.