Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Construction of a 2.8-megabase yeast artificial chromosome contig and cloning of the human methylthioadenosine phosphorylase gene from the tumor suppressor region on 9p21.
|
7604019 |
1995 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Recent evidence suggests that homozygous loss of the interferon (IFN) and methylthioadenosine phosphorylase (MTAP) genes located on 9p and a tumor suppressor gene closely linked to them is associated with acute lymphoblastic leukemia and with gliomas.
|
7683574 |
1993 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
5'-Deoxy-5'methylthioadenosine phosphorylase (MTA-Pase) gene is localized at the 9p21 region linked to the recently identified putative tumor suppressor gene, p16INK4, which appears implicated in the control of cell division cycle.
|
7898924 |
1995 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Because the MTAP gene is located adjacent to the tumor-suppressor gene p16 on chromosome 9p21 and more than 60% of T-cell ALL (T-ALL) patients have deletion in the p16 gene, we examined the status of the MTAP gene in T-ALL patients.
|
8874207 |
1996 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The gene for methylthioadenosine phosphorylase (MTAP), a purine and methionine metabolic enzyme, resides approximately 100 Kb telomeric to the p16INK4a gene and is frequently co-deleted with the tumor suppressor gene in a variety of cancers.
|
9426690 |
1998 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Homozygous deletions of the tumor suppressor gene p16INK4A and deficiency of methylthioadenosine phosphorylase (MTAP), both located on chromosome 9p21, have been independently reported in non-small cell lung cancer (NSCLC).
|
9840931 |
1998 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Quantitative PCR showed chromosome 9p deletions including p16 tumor suppressor gene (2 of 7 tumors) and MTAP gene (3 of 7).
|
10329596 |
1999 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Many tumors lacking MTAP have been found to homozygously delete the chromosome 9p region containing the p16 tumor suppressor gene.
|
10803528 |
2000 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The MTAP gene is commonly deleted in osteosarcoma patient samples, leading to an absence of mRNA and protein expression; these results indicate that inhibitors of de novo purine synthesis or methionine depletion may be effective as treatments for osteosarcoma patients whose tumors fail to express MTAP.
|
11895909 |
2002 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
These results indicate that MTAP has tumor suppressor activity and suggest that its effects may be mediated by altering intracellular polyamine pools.
|
12438261 |
2002 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In summary, we demonstrate significant inverse correlation between MTAP protein expression and progression of melanocytic tumors as the amount of MTAP protein staining decreases from benign melanocytic nevi to metastatic melanomas.
|
12875987 |
2003 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
An in vivo study using HT-1080 cell tumors with and without MTAP expression confirmed that tumors lacking MTAP were more sensitive to L-alanosine than tumors expressing MTAP.
|
15301428 |
2004 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Hemizygous deletion of the region harbouring the CDKN2A and CDKN2B loci was identified in two tumours by means of fluorescent in situ hybridisation and MTAP was present by immunostaining in all but one tumour analysed.
|
15305192 |
2004 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Recently, several groups including our own have shown that MTAP serves as a tumour suppressor gene.
|
15492751 |
2005 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Given the recently proposed tumor suppressor activity of MTAP, our observations can be relevant to the elucidation of the molecular mechanisms of multistep hepatocarcinogenesis.
|
15511635 |
2004 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We have shown previously that MTAP can act as a tumor suppressor gene and that its tumor suppressor function is related to its effect on polyamine homeostasis.
|
15534104 |
2004 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
These results suggest that MTAP expression is lost in approximately 30% of infiltrating pancreatic cancers and in a lower percentage of other periampullary neoplasms, that this loss is the result of homozygous deletions encompassing both the MTAP and p16INK4A/CDKN2A genes.
|
15662124 |
2005 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Methylthioadenosine phosphorylase (MTAP) involved in the metabolism of purine and polyamine has been known to be deficient in a variety of tumors.
|
15753993 |
2005 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The homozygous co-deletion of MTAP, encoding the enzyme methylthioadenosine phosphorylase, in approximately 90% of mesotheliomas with P16/CDKN2A loss has potential therapeutic applications because MTAP-deficient tumors may be responsive to inhibitors of de novo AMP synthesis.
|
15950811 |
2005 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The gene that encodes methylthioadenosine phosphorylase (MTAP), an enzyme involved in adenine and methionine salvage pathways, is located on chromosome 9p21 telomeric to the p16INK4A/CDKN2A tumor suppressor gene.
|
16224217 |
2005 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
To determine the methylthioadenosine phosphorylase (MTAP) gene alterations in mantle cell lymphoma (MCL) and to investigate whether the targeted inactivation of the alternative de novo AMP synthesis pathway may be a useful therapeutic strategy in tumors with inactivation of this enzyme.
|
16778103 |
2006 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Systemic MTA accumulation is implicated as the tumor-suppressive metabolite because MTDIA is effective for in vivo treatment of A549 MTAP(-/-) and H358 MTAP(+/+) tumors.
|
21135097 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These data further indicate MTAP as a tumor suppressor in HCC, and MTA as a potential biomarker for HCC progression.
|
21356366 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The present study suggests that MTAP plays an important role in the regulation of gastric carcinogenesis and, in particular, that MTAP loss is implicated in some way with tumor growth via the modulation of cellular properties, which, in turn, suggests that MTAP has therapeutic applications.
|
21412930 |
2011 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
This therapeutic approach can be applied to other MTAP-deficient human cancers as deletion or hypermethylation of the MTAP gene occurs in a broad spectrum of tumors at high frequency.
|
22252602 |
2012 |