Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UMLS:C0033036 (APC)
 10,214 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The APC gene plays a major role in human colon carcinogenesis. We determined the genomic structure of the rat Apc gene, and we analyzed mutations in colon tumors induced in F344 rats by 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) and 2-amino-3-methylimidazo[4,5-f]quinoline (IQ), potent carcinogens contained in ordinary daily human food. Of eight PhIP-induced tumors, one tumor had two Apc mutations, two tumors had a mutation with loss of the normal allele, and one had a mutation. Two of the above five mutations were at nucleotide 1903, one at 2605, and two at 4237, all being a deletion of a guanine base at the 5'-GGGA-3' site and resulting in truncation of the APC protein. Of 13 IQ-induced tumors, 2 had an Apc mutation with loss of the normal allele. The two mutations were a missense mutation (T-->C) at nucleotide 1567 and a nonsense mutation (C-->T) at 2761. Alteration of the Apc gene was shown to play a more important role in PhIP-induced than in IQ-induced rat colon carcinogenesis. PhIP-induced tumors are characterized by their specific and unique mutation, which may be useful for mutational fingerprinting of human cancers.
 ...
PMID:Specific 5'-GGGA-3'-->5'-GGA-3' mutation of the Apc gene in rat colon tumors induced by 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine. 784 77

The cooked meat mutagen 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) produces tumors at multiple sites in the F344 rat, including adenocarcinomas of the colon. In the present study, the development of IQ-induced colorectal tumors was shown to be accompanied by the progressive inhibition of programmed cell death. This was associated with increased expression of the antiapoptosis protein Bcl-2 and decreased expression of bax, a known activator of apoptosis. Carcinomas bearing high levels of bcl-2 expression exhibited low levels of p53, the tumor suppressor protein that in some circumstances has been shown to down-regulate bcl-2. Because they lack mutations in the genes commonly associated with increased cell proliferation (APC, Ki-ras, and p53) and show no evidence of microsatellite instability, IQ-induced colon tumors might arise via the deregulation of bcl-2 expression, leading to inhibition of programmed cell death.
 ...
PMID:Inhibition of apoptosis in colon tumors induced in the rat by 2-amino-3-methylimidazo[4,5-f]quinoline. 881 12

Heterocyclic amines are potent mutagens and carcinogens formed in cooked protein rich foods. In this study, we screened liver tumors induced by 2-amino-3,4-dimethylimidazo[4,5-f]quinoline (MeIQ) in CDF1 mice for beta-catenin and APC mutations and other genetic alterations shown to occur in human hepatocellular carcinomas (HCC), including mutations in the p53 and H-ras genes, c-myc amplification and E-cadherin promoter methylation. SSCP followed by direct DNA sequencing revealed mutations in exon 2 of the beta-catenin gene in 2 of 16 liver tumors (12.5%). Promoter methylation of the E-cadherin gene was detected in one liver tumor induced by MeIQ. There were no mutations in the mutation cluster region of the APC gene, in exons 5-8 of the p53 gene, or in codons 12, 13 and 61 of the H-ras gene, nor c-myc amplification in any of liver tumors induced by MeIQ. These data indicate that except for the occasional disruption of the Wnt pathway through beta-catenin mutations, the genetic pathways involved in the development of HCC differ significantly between human liver cancer and tumors induced in mice by MeIQ, but do not rule out the possibility that heterocyclic amines constitute a carcinogenic risk factor in humans.
 ...
PMID:Beta-catenin mutations in liver tumors induced by 2-amino-3,4-dimethylimidazo[4,5-f]quinoline in CDF1 mice. 1289 27

Chloroquine (CQ) distribution in tissues of acutely poisoned mice was demonstrated by immunohistochemistry using anti-CQ polyclonal antibodies (PAC). PAC recognized 4-amino-7-chloro-quinoline structure and sufficiently reacted with CQ and CQ's metabolite bisdesethyl-chloroquine. In the brain, CQ and its metabolites (CQs) localized in the region of the choroids plexus, indicating an important role in the blood-cerebrospinal barrier system. In the heart, most regions showed diffused positive staining, and relatively strong reaction was observed in Purkinje cells, indicating an important role in acute CQ toxicity. In the lungs, CQs were observed in the bronchial epithelium, type II pneumocytes, and on the surface of alveolar walls. It was suggested that CQs were excreted to the alveolar wall with surfactant phospholipids, which are produced by type II pneumocytes. In the liver, CQs were concentrated in the centrolobular area rather than in the periportal area, in agreement with CQ's metabolic pathway. In the kidneys, tubular cells were strongly stained compared to glomerular capsules, and the distal part of renal tubules was better stained than the proximal tubules. These findings suggested that CQs were predominantly excreted or reabsorbed through the distal tubules and the collecting duct. Distribution of CQs in tissues presented here were mostly consistent with the physico-chemical properties of CQ and its metabolites. However, the elucidation of CQs' localization in Purkinje cells remains open. Further experimental studies at the level of microorganella will be needed to clarify the present result.
 ...
PMID:Immunohistochemical demonstration of the distribution of chloroquine (CQ) and its metabolites in CQ-poisoned mice. 1759 11

Polycyclic aromatic hydrocarbons (PAHs) are believed to be responsible for the formation of organic haze layers in Titan's atmosphere, but the nature of PAHs on Titan and their formation and growth mechanisms are not well understood. Considering the high abundance of nitrogen in Titan's atmosphere, it is likely that the haze layers hold not only pure hydrocarbon PAHs but also their nitrogenated analogs, N-containing polycyclic aromatic compounds (N-PACs) with 'hetero' N atoms in aromatic rings. Laboratory studies of Titan's tholins also support the hypothesis that, together with pure PAHs and their cations, N-PACs may be the fundamental building blocks of microphysical tholin particles. In the present work, we carried out ab initio quantum chemical calculations of potential energy surfaces for various reaction mechanisms of incorporation of nitrogen atoms into aromatic rings of polycyclic aromatic compounds, which may lead to the formation of N-PACs under the low-temperature and low-pressure conditions of Titan's atmosphere. This includes mechanisms analogous to the Ethynyl Addition Mechanism (EAM) recently proposed by us for the growth of PAH by sequential C2H additions to benzene. We consider consecutive C2H and CN additions to C6H6, C6H6 + CN --> C6H5CN + H, C6HCN + C2H --> C6H4(CN)(C2H) + H, C6H5CN + CN --> C6H4(CN)2 + H, C6H4(CN)(C2H) + C2H --> 2-aza-4-ethynyl-1-naphthyl/2-aza-1-ethynyl-4-naphthyl, C6H4(CN)2 + C2H --> C6H4(CN)(NCCCH), and C6H4(CN)(NCCCH) + C2H --> 1,4-diethynylphthalazine. Although these reactions are found to be barrierless and exothermic and therefore feasible at low temperatures, the steps leading to the aza-ethynyl-naphthyl radicals, C6H4(CN)(NCCCH), and 1,4-diethynylphthalazine can give N-PACs as final products only upon their collisional or radiational stabilization. Alternatively, an N-PAC can be synthesized via the reaction of 2-methyleneaminobenzonitrile with C2H, producing 4-ethynyl-quinoline + H without an entrance barrier via a three-step sequence including C2H addition to C of CN, ring closure, and H elimination. 2-Methyleneaminobenzonitrile itself can be formed in the reaction of methyleneaminobenzene with cyano radical, C6H5(NCH2) + CN --> C6H5(NCH2)(CN) --> C6H4(NCH2)(CN) + H, which also does not have any entrance barrier. Methyleneaminobenzene can be produced through recombination of phenyl and methylene-amidogen radicals followed by collisional stabilization of the product, via the barrierless C6Hs + CH3N --> C6Hs(NCH3) --> C6H5(NCH2) + H reaction, or in the reaction of phenyl with methyleneimine, C6H5 + CH2NH --> C6Hs(NHCH3) --> C6H5(NCH2) + H. The latter would be slow at low-temperature conditions owing to the barriers of 4.5 and 2.8 kcal mol(-1) relative to the initial reactants, but feasible if the reactants possess sufficient internal energy to overcome these barriers. We anticipate that the presented mechanisms are viable to form N-PACs in hydrocarbon and nitrogen rich, low temperature atmospheres of planets and their moons such as Titan.
 ...
PMID:Mechanisms of formation of nitrogen-containing polycyclic aromatic compounds in low-temperature environments of planetary atmospheres: a theoretical study. 2130 61

A selective KGFR tyrosine kinase inhibitor, N-ethylamino-2-oxo-1,2-dihydro-quinoline-3-carboxamide, was synthesized and its possible inhibitory effects on the development of colon polyps and colorectal tumors was examined in APC(Min/+) mice, a mouse model of human intestinal familial adenomatous polyposis. The present study shows for the first time that a dietary administration of a selective KGFR tyrosine kinase inhibitor lacks the overt-toxicities and significantly reduced the growth of small intestinal polyps in both male and female APC(Min/+) mice. This inhibition of polyp growth appears to occur at a greater extent in female mice.
 ...
PMID:Synthesis and in vivo evaluation of N-ethylamino-2-oxo-1,2-dihydro-quinoline-3-carboxamide for inhibition of intestinal tumorigenesis in APC(Min/+) mice. 2450 28

Anaerobic bottle experiments were conducted in parallel for 120 consecutive days to perform the bioaugmentation hydrolysis of selected nitrogen heterocyclic compounds (NHCs) in coal gasification wastewater. Due to enhancement with PAC and Fe(OH)3@PAC, quinoline, pyridine, and indole were hydrolyzed more effectively. The addition of PAC and Fe(OH)3@PAC improved the coagulation capacity of microorganisms, which laid a solid foundation for the removal of selected NHCs and the adverse environmental conditions. Anaerobic degradation of the NHCs occurred first through hydrogenation, then through the opening of the nitrogen heterocycles, followed by the release of ammonia nitrogen and finally the opening of the benzene rings. Enriched Acinetobacter, Levilinea, Comamonas, and Longilinea were the main functional groups responsible for the anaerobic biodegradation of the selected NHCs.
 ...
PMID:Anaerobic bioaugmentation hydrolysis of selected nitrogen heterocyclic compound in coal gasification wastewater. 3070 40