DPC4, a candidate tumor suppressor gene at human chromosome 18q21. 1

SA Hahn, M Schutte, ATMS Hoque, CA Moskaluk… - …, 1996 - science.sciencemag.org
About 90 percent of human pancreatic carcinomas show allelic loss at chromosome 18q. To
identify candidate tumor suppressor genes on 18q, a panel of pancreatic carcinomas were
analyzed for convergent sites of homozygous deletion. Twenty-five of 84 tumors had …

Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma

C Caldas, SA Hahn, LT Da Costa, MS Redston… - Nature …, 1994 - nature.com
The MTS1 gene on chromosome 9p21 encodes the p16 inhibitor of cyclinD/Cdk-4
complexes, and is deleted or mutated in a variety of tumour types. We found allelic deletions
of 9p21–p22 in 85% of pancreatic adenocarcinomas. Analysis of MTS1 in pancreatic …

DPC4 gene in various tumor types

…, D Sidransky, RA Casero, PS Meltzer, SA Hahn… - Cancer research, 1996 - AACR
We recently identified a novel tumor-suppressor gene, DPC4, at chromosome 18q21. 1 and
found that both alleles of DPC4 were inactivated in nearly one-half of the pancreatic
carcinomas. Here, we analyzed 338 tumors, originating from 12 distinct anatomic sites, for …

Tumor-suppressive pathways in pancreatic carcinoma

E Rozenblum, M Schutte, M Goggins, SA Hahn… - Cancer research, 1997 - AACR
During tumorigenesis, positive selection is exerted upon those tumor cells that alter rate-
limiting regulatory pathways. A corollary of this principle is that mutation of one gene
abrogates the need for alteration of another gene in the same pathway and also that the …

Abrogation of the Rb/p16 tumor-suppressive pathway in virtually all pancreatic carcinomas

…, W Hilgers, SK Rabindran, CA Moskaluk, SA Hahn… - Cancer research, 1997 - AACR
The Rb/p16 tumor-suppressive pathway is abrogated frequently in human tumors, either
through inactivation of the Rb or p16 INK4a/CDKN2/MTS1 tumor-suppressor proteins, or
through alteration or overexpression of the cyclin D1 or cyclin-dependent kinase 4 …

Evaluation of candidate tumour suppressor genes on chromosome 18 in colorectal cancers

…, C Lengauer, FS Leach, M Schutte, SA Hahn… - Nature …, 1996 - nature.com
Chromosome deletions are the most common genetic events observed in cancer 1–4. These
deletions are generally thought to reflect the existence of a tumour suppressor gene within
the lost region 5. However, when the lost region does not precisely coincide with a …

BRCA2 germline mutations in familial pancreatic carcinoma

SA Hahn, B Greenhalf, I Ellis… - Journal of the …, 2003 - academic.oup.com
Background: Although as many as 10% of pancreatic cancer cases may have an inherited
component, familial pancreatic cancer has not been linked to defects in any specific gene.
Some studies have shown that families with germline mutations in the breast cancer …

Detection of K-ras mutations in the stool of patients with pancreatic adenocarcinoma and pancreatic ductal hyperplasia

C Caldas, SA Hahn, RH Hruban, MS Redston, CJ Yeo… - Cancer research, 1994 - AACR
Pancreatic adenocarcinoma is the fifth leading cause of cancer death in the United States.
Mutations in the K-ras oncogene occur in 85% of pancreatic adenocarcinomas and have
also been identified in 75% of pancreatic ducts with mucinous cell hyperplasia seen in …

Allelotype of pancreatic adenocarcinoma using xenograft enrichment

SA Hahn, AB Seymour, ATMS Hoque, M Schutte… - Cancer research, 1995 - AACR
Abstract p53 and MTS1 are known to be mutationally inactivated in pancreatic
adenocarcinoma. Other tumor suppressor genes are likely also to play a role. To define
chromosomal arms which may harbor additional tumor suppressor genes, we performed an …

Smad4/DPC4-mediated tumor suppression through suppression of angiogenesis

…, NP Bouck, B Sipos, SA Hahn… - Proceedings of the …, 2000 - National Acad Sciences
Smad4/DPC4 (deleted in pancreatic carcinoma, locus 4) is a tumor suppressor gene lost at
high frequency in cancers of the pancreas and other gastrointestinal organs. Smad4
encodes a key intracellular messenger in the transforming growth factor β (TGF-β) signaling …