Biomedical subjects

Xiangrong Li

Publications and source records attributed to Xiangrong Li.

8 recordsLinked to original sources

PubMed2006

Brain magnetic resonance imaging and manganese concentrations in red blood cells of smelting workers: search for biomarkers of manganese exposure.

The MRI technique has been used in diagnosis of manganism in humans and non-human primates. This cross-sectional study was designed to explore whether the pallidal signal intensity in T1-weighted MRI correlated with Mn levels in the blood compartment among Mn-exposed workers and to understand to what extent the MRI signal could reflect Mn exposure. A group of 18 randomly selected male Mn-exposed workers of which 13 were smelting workers with high exposure (mean of airborne Mn in work place: 1.26 mg/m3; range: 0.31-2.93 mg/m3), and 5 power distribution control workers with low exposure (0.66 mg/m3 and 0.23-0.77 mg/m3) from a ferroalloy factory, and another group of 9 male subjects as controls from a non-smelting factory who were office or cafeteria workers (0.01 mg/m3 and 0-0.03 mg/m3) were recruited for neurological tests, MRI examination, and analysis of Mn in whole blood (MnB), plasma (MnP) or red blood cells (MnRBC). No clinical symptoms and signs of manganism were observed among these workers. MRI data showed average increases of 7.4% (p<0.05) and 16.1% (p<0.01) in pallidal index (PI) among low- and high-exposed workers, respectively, as compared to controls. Fourteen out of 18 Mn-exposed workers (78%) had intensified PI values, while this proportion was even higher (85%) among the high Mn-exposed workers. Among exposed workers, the PI values were significantly associated with MnRBC (r=0.55, p=0.02). Our data suggest that the workers exposed to airborne Mn, but without clinical symptoms, display an exposure-related, intensified MRI signal. The MRI, as well as MnRBC, may be useful in early diagnosis of Mn exposure.

Adult↗

PubMed2006

Scalability of the surface-based DNA algorithm for 3-SAT.

Since Adleman first proposed DNA computing for the Hamiltonian path problem, several authors have reported DNA computing for 3-SAT. Previous research presented DNA computing on surfaces and demonstrated how to solve a four-variable four-clause instance of 3-SAT, and claimed that the surface-based approach was designed to scale up to larger problems. In this paper we establish an error model for the incomplete "mark" and imperfect "destroy" operations. By using the error model we argue that no matter how large the "mark" and "destroy" rates are we can always give satisfiable instances of 3-SAT such that no DNA strands remain on the surface at the end of the computation. By the surface-based approach the satisfiable instances of 3-SAT would be misdetermined to be unsatisfiable. Thus, the error leads to an incorrect result of the SAT computation. Furthermore, given the "mark" rate p and the "not-destroy" rate rho, we find that the approach can only solve at most N-variable instances of 3-SAT problems, where N=[(2+beta(2)+2+2 square root beta (2))/beta(2)] in which beta=1-1/(p+rhoq) and q=1-p and [a] is the greatest integer less than a or equal to a.

Algorithms↗

PubMed2006

Activation of kinase pathways in MCF-7 cells by 17beta-estradiol and structurally diverse estrogenic compounds.

17beta-Estradiol (E2) activates non-genomic pathways in MCF-7 cells, and this study investigates the effects of structurally-diverse estrogenic compounds on activation of mitogen-activated protein kinase (MAPK), phosphatidylinositol-3-kinase (PI3-K), protein kinase C (PKC), PKA, and calcium calmodulin-dependent kinase IV (CaMKIV). Activation of kinases was determined by specific substrate phosphorylation and transactivation assays that were diagnostic for individual kinases. The compounds investigated in this study include E2, diethylstilbestrol (DES), the phytoestrogen resveratrol, and the following synthetic xenoestrogens, bisphenol-A (BPA), nonylphenol, octylphenol, endosulfan, kepone, 2,2-bis(p-hydroxyphenyl)-1,1,1-trichloroethane (HPTE), and 2',3',4',5'-tetrachloro-4-biphenylol (HO-PCB-Cl(4)). With the exception of resveratrol, all the compounds activated PI3-K and MAPK. Activation of PKC by the xenoestrogens was structure-dependent since resveratrol, kepone and HO-PCB-Cl(4) were inactive and only minimal activation of PKA was observed. CaMKIV was activated only by E2 and DES, and HO-PCB-Cl(4) was a potent inhibitor of CaMKIV-dependent activity. These results demonstrate that activation of estrogen receptor-alpha-mediated non-genomic pathways by estrogenic compounds in MCF-7 cells is structure-dependent and can result in activation or inhibition of kinase activities.

Benzhydryl Compounds↗

PubMed2005

The surface-based approach for DNA computation is unreliable for SAT.

Previous research presented DNA computing on surfaces, which applied to each clause three operations:"mark","destroy", and "unmark", and demonstrated how to solve a four-variable four-clause instance of the 3-SAT. It was claimed that only the strands satisfying the problem remained on the surface at the end of the computation and the surface-based approach was capable of scaling up to larger 3-SAT problems. Accordingly, the identities of the strands were only determined in the"readout" step for the correct solutions to the problem without checking if the strands really satisfied the problem. Thus, based on the claim above, the surface-based approach became a polynomial-time algorithm. In this paper, we show that for some instance of SAT, at the end of the computation all the remaining strands falsify the instance. However, by the previous claim all the strands falsifying the problems would be regarded as the correct solutions to the problems. Therefore, the DNA computing on surfaces is unreliable. For this reason, it is necessary to add a "verify" step after the "readout" step to check if the strands remaining on the surface at the end of the computation really satisfy the problem.

Algorithms↗

PubMed2004

Childhood adiposity as a predictor of cardiac mass in adulthood: the Bogalusa Heart Study.

BACKGROUND: The association between left ventricular hypertrophy, an independent predictor of cardiovascular (CV) morbidity and mortality, and CV risk factors has been well documented in childhood and in adulthood. However, information on the relationship between left ventricular mass (LVM) in adults and longitudinal measurements of CV risk factors from childhood to adulthood is limited. METHODS AND RESULTS: LVM was obtained with 2D M-mode echocardiography in a community-based sample of 467 young adults (71% white and 29% black) aged 20 to 38 years who were examined an average of 6 times for CV risk factors from childhood to adulthood. The average follow-up period was 21.5 years. The cumulative burden of each risk factor was calculated as the area under the curve for each individual. Compared with whites, blacks had greater LVM (indexed to height(2.7); P<0.05). In multiple regression analyses, adiposity (measured as body mass index) in childhood, adiposity and systolic blood pressure in adulthood, and the cumulative burden of adiposity and systolic blood pressure from childhood to adulthood were significant predictors of LVM index in young adults. CONCLUSIONS: These observations, by showing that adiposity beginning in childhood is a consistent predictor of LVM in young adults, underscore the importance of obesity in the development of left ventricular hypertrophy and the need for early prevention.

Adolescent↗

PubMed2004

Hormonal regulation of lactate dehydrogenase-A through activation of protein kinase C pathways in MCF-7 breast cancer cells.

Lactate dehydrogenase A (LDH-A) is hormonally regulated in rodents, and increased expression of LDH-A is observed during mammary gland tumorigenesis. The mechanisms of hormonal regulation of LDH-A were investigated using a series of deletion and mutant constructs derived from the rat LDH-A gene promoter. Results of these studies show that constructs containing the -92 to -37 region of the LDH-A promoter are important for basal and E2-induced transactivation, and mutation of the consensus CRE motif within this region results in significant loss of basal activity and hormone-responsiveness. Gel mobility shift assays using nuclear extracts from MCF-7 cells show that both CREB and ATF-1 interact with the CRE. Studies with kinase inhibitors show that E2-induced activation of this CRE is dependent on protein kinase C, and these data indicate that LDH-A is induced through a non-genomic pathway of estrogen action.

Animals↗

PubMed2003

Hairpin formation in DNA computation presents limits for large NP-complete problems.

Recently, several DNA computing paradigms for NP-complete problems were presented, especially for the 3-SAT problem. Can the present paradigms solve more than just trivial instances of NP-complete problems? In this paper we show that with high probability potentially deleterious features such as severe hairpin loops would be likely to arise. If DNA strand x of length n and the 'complement' of the reverse of x have l match bases, then x forms a hairpin loop and is called a (n,l)-hairpin format. Let gamma=2l/n. Then gamma can be considered as a measurement of the stability of hairpin loops. Let p(n,l) be the probability that a n-mer DNA strand is a (n,l)-hairpin format, and q(n,l)((m)) be the probability that m ones are chosen at random from 4(n) n-mer oligonucleotides such that at least one of the m ones is a (n,l)-hairpin format. Then, q(n,l)((m))=1-(1-p(n,l))(m)=mp(n,l). If we require q(n,l)((m))<a, where a<1, then m<ln(1-a)/ln(1-p(n,l))=a/p(n,l). It means that we can only solve the instances of size m of NP-complete problems. Clearly the greater p(n,l), the smaller m, and the smaller a the smaller m. In this paper, we show p(n,l) is high. Therefore, the present DNA computing paradigms cannot solve large NP-complete problems. For example, if n=20, used in Adleman and Lipton's paradigm, gamma=50% and a=50%, then m is almost 12.

Algorithms↗

PubMed2002

Estrogen regulation of c-fos gene expression through phosphatidylinositol-3-kinase-dependent activation of serum response factor in MCF-7 breast cancer cells.

17Beta-estradiol (E2) induces proliferation and c-fos gene expression in MCF-7 cells and both responses are partially blocked by wortmannin and LY294002 which are inhibitors of phosphatidylinositol-3-kinase (PI3-K). Analysis of the c-fos gene promoter shows that the effects of wortmannin and LY294002 are associated with inhibition of E2-induced activation through the serum response factor (SRF) motif within the proximal serum response element at -325 and -296. E2 activates constructs containing multiple copies of the SRF (pSRF) and a GAL4-SRF fusion protein; these responses are accompanied by PI3-K-dependent phosphorylation of Akt and inhibited by wortmannin/LY294002, the antiestrogen ICI 182780, but not by the mitogen-activated protein kinase kinase (MAPKK) inhibitor PD98059. Using a series of kinase inhibitors and dominant negative kinase expression plasmids, it was shown that the non-genomic activation of SRF by E2 was associated with src-ras-PI3-K pathway, thus, demonstrating hormonal activation of the SRE through src-ras activation of both PI3-K- and MAPK-dependent signaling pathways.

Androstadienes↗