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Biomedical subjects

Jianjun Zhang

Publications and source records attributed to Jianjun Zhang.

At least 19 recordsLinked to original sources

Plasma signals of lung tumor promotion for molecular cancer prevention.

Predicting lung cancer risk would enhance prevention trials. Although the Canakinumab Anti-inflammatory Thrombosis Outcome Study (CANTOS) trial demonstrated reduced lung cancer incidence with interleukin (IL)-1β inhibition, the high number needed to treat (NNT) to prevent lung cancer limits its use in unselected populations. Using machine learning, we identified a 14-protein plasma signature predicting lung cancer more than 5 years before diagnosis. The signature, validated across eight cohorts, was elevated in current smokers and individuals exposed to particulate matter (PM) and linked to lung myeloid and alveolar cells. In epidermal growth factor receptor (EGFR)-driven lung adenocarcinoma, diverse epithelial lineages converged on a keratin8+/claudin4+ alveolar transitional state (KAC), whose transcriptional programs correlated with signature emergence. Components of the signature were induced by PM, oncogenic EGFR, or IL-1β, whereas IL-1β inhibition restrained PM-driven KAC expansion and early tumorigenesis. In CANTOS, the signature identified individuals who seemed to benefit more from anti-IL-1β therapy, lowering the NNT threshold and nominating circulating signals of tumor promotion for prevention.

Humans↗

FOXM1-Specific TCR-Engineered T Cells Target Non-Small Cell Lung Cancer.

FOXM1 is highly expressed in various cancer types and considered a key driver of cancer progression. Accordingly, we evaluated the immunogenicity of FOXM1 and investigated the feasibility of targeting this transcription factor using T-cell receptor (TCR) engineering. We identified epitopes derived from FOXM1 which were immunogenic on HLA-A*02:01, HLA-A*24:02, and HLA-A*23:01, endogenously processed and presented, and resulted in T-cell activation and cytotoxic T-cell responses. Following the generation of TCR-T cells, sensitivity and specificity were confirmed by peptide dose-response and X-scan, respectively. Most importantly, adoptive transfer of TCR-engineered T cells led to a significant reduction in tumor growth, as well as significantly prolonged survival in a tumor-bearing immunocompromised murine model. Our studies confirm the immunogenicity of FOXM1 and feasibility of targeting this antigen using TCR engineering.

Forkhead Box Protein M1↗

Distinct Clinicogenomic Features and Immunotherapy Associations in Pulmonary Sarcomatoid Carcinoma: A Multicenter Retrospective Study.

INTRODUCTION: Pulmonary sarcomatoid carcinoma (PSC) is a rare NSCLC subtype with poor prognosis. Outcomes to immune checkpoint inhibitors (ICIs) and genomic features in PSC remain underexplored compared with other NSCLC subtypes. METHODS: Patients from three institutions and the National Cancer Database (NCDB) with metastatic NSCLC treated with ICI alone or with chemotherapy were identified. Clinicogenomics and treatment outcomes were compared across PSC, lung adenocarcinoma (LUAD), and lung squamous cell carcinoma (LUSC). RESULTS: We analyzed 4841 patients including 165 PSC cases treated with ICI-based therapy from three institutions and 201 PSC from NCDB. In MDACC, 65 (4.3%) were PSC, 1138 (75.1%) LUAD, and 312 (20.6%) LUSC. Patients with PSC were older and more likely to present with metastatic disease. In both the MDACC and NCDB cohorts, ICIs resulted in better outcomes for patients with PSC compared with chemotherapy. In these patients, there was no difference in outcome between ICI-monotherapy and ICI-chemotherapy. Across the three institutional cohorts, 37% to 43% of patients with PSC who received ICIs were responders, compared with 26% to 29% in LUAD and 22% to 46% in LUSC (p < 0.05). Improved ICI outcomes in PSC appeared driven by high PD-L1 (&#x2265;50% in 73%-77% cases). Among patients with high PD-L1, response rates were similar across histologic subtypes. Conversely, TMB was similar in PSC compared with LUAD or LUSC and was not associated with ICI outcomes. Across cohorts, PSC tumors were enriched for TP53, NF1, NF2, and NRAS, with relative depletion of STK11 and KEAP1 compared with LUAD. Case observation revealed relatively better outcomes to ICI than targeted therapies in patients with PSC with MET exon 14 skipping or KRAS G12C. CONCLUSION: PSC exhibits improved outcomes to ICI relative to other therapies, potentially driven by high PD-L1 expression. Genomic analysis highlights a distinct genomic landscape of PSC when compared with LUAD.

Humans↗

Dactylorhin B reduces toxic effects of beta-amyloid fragment (25-35) on neuron cells and isolated rat brain mitochondria.

beta-amyloid is strongly implicated in Alzheimer's pathology, and mitochondria play an important role in neurodegenerative disorders. Dactylorhin B [short for bis(4-beta-D-glucopyranosyloxybenzyl)-2-beta-D-glucopyranosyl-2-isobutyltartrate (DHB)] is an active compound isolated from Coeloglossum viride. (L.) Hartm. var. bracteatum (Willd.) and may have neuroprotective effects. In the present study, we investigated the damage of rat brain mitochondrial function induced by beta-amyloid and the protective effect of DHB. Isolated rat brain mitochondria were incubated with amyloid-beta peptide (Abeta)(25-35) alone or together with DHB. reactive oxygen species production, pyruvate dehydrogenase complex activity, alpha-ketoglutarate dehydrogenase complex activity, cytochrome c oxidase activity, mitochondrial swelling, mitochondrial membrane potential and the release of cytochrome c from mitochondria were measured. Data showed that Abeta(25-35) directly disrupted mitochondrial function, inhibited the key enzymes and contributed to apoptosis and the deficiency of energy metabolism. Co-incubation of DHB attenuated Abeta(25-35)-induced pathological changes. The significance of DHB in the management of mitochondria-related disorders is discussed.

Adenosine Triphosphatases↗

Two chiral metal clusters derived from nucleophilic addition of L-proline to di-2-pyridyl ketone.

In the presence of cobalt (nickel) acetate, a chiral tetrahedral intermediate ligand of (S)-(C5NH4)2C(OH)(C4NH7CO2H) was first formed from the nucleophilic addition of l-proline as a secondary amine to ketone (di-2-pyridyl ketone). Based on the ligand synthesized in situ, two chiral tetranuclear isomorphous complexes 1 and 2 with the formula {Na[M4L3(OAc)3](ClO4)(1.5)(H2O)(1.5)}(ClO4)(OH)(0.5).3H2O (M = Co, Ni) have been achieved. The Co4 cluster (1) behaves as a ferromagnet.

Journal Article↗

Nimodipine treatment to assess a modified mouse model of intracerebral hemorrhage.

One of the main limitations of intracerebral hemorrhage (ICH) research is lack of reproducible animal models. ICH appears to be associated with a volume of edema and ischemic injury surrounding the hematoma that may be reduced by nimodipine due to its vasodilating and cytoprotective effects. The present study was designed to produce a modified ICH model in mice based on the double-injection method initially developed by Dr. Belayev and accordingly performed in 3 groups: to evaluate this model itself and to assess the pharmacological effects of nimodipine in this model, respectively. In 80 ICR mice (32 +/- 3 g), ICH was induced by 30 microL whole blood injection into the caudate nucleus. ICH animals were then randomly received either nimodipine (5 mg/kg) or vehicle intraperitoneal injection just before and every 24 h after ICH (total of four times). The changes for cortical blood flow (CBF) were studied by the technique of Laser Doppler Perfusion Measure (LDPM). Animals were rated on a behavioral test and sacrificed at 72 h after ICH. The brains were removed, and hematoma volume and brain edema were subsequently determined. Due to the vasodilating effect of nimodipine, ICH animals treated with nimodipine had marked improved CBF accompanied by the improvement of forelimb placing performance compared with vehicle-treated ICH animals, though there was no marked difference in the hematoma volume and brain water content. In conclusion, the 30 microL whole blood injection closely mimicked natural ischemic events that occurred in human massive ICH and confirmed the anti-ischemia effect of nimodipine. This study suggested that nimodipine could be markedly effective to reduce edema and hematoma volume when administered in combination with other neuroprotective agents because ICH can induce brain injury by multiple mechanisms.

Analysis of Variance↗

Differences in breast cancer mortality worldwide: unsolved problems.

Breast cancer mortality remains a major cause of female mortality. Between 1970 and 2000 both important increases and decreases in breast cancer mortality rates occurred. Large differences in breast cancer mortality exist among countries worldwide. Contradictory findings concerning the role of lifestyle, especially nutrition, remain to be explained. Possible explanations for the observed mortality differences will be explored. Breast cancer mortality rates have been correlated with other causes of mortality; both cancer and noncancer, using data obtained from 47 countries worldwide (World Health Organization). They have also been correlated with dietary data, especially concerning fat (animal and vegetal) intake (Food and Agricultural Organization). Highly significant correlations existed between breast cancer mortality and mortality from other cancers (e.g. colon, stomach) obtained from both sexes. These correlations have been confirmed over a period of more than 40 years. Highly significant positive correlations also existed with the intake of animal (saturated) fat, covering a period of 30 years. In multivariate regression, only the relationship with the colon, prostate cancer and total energy intake remained significant. Ecological data point to nutritional factors, especially animal fat, as major promoters of breast cancer mortality worldwide. This contrasts with the results of most cohort studies. These contradictory results and the relationship between breast cancer mortality and other causes of mortality remain to be explained. More refined and standardized dietary data are necessary.

Aged↗

[Interrelations between plant communities and environmental factors of wetlands and surrounding lands in mid- and lower reaches of Tarim River].

A total of 16 quadrants of wetlands and surrounding lands in the mid- and lower reaches of Tarim River were surveyed, and the data about the characteristics of plant communities and environmental factors were collected and counted. By using PCA (principal component analysis) ordination and regression procedure, the distribution patterns of plant communities and the relationships between the characteristics of plant community structure and environmental factors were analyzed. The results showed that the distribution of the plant communities was closely related to soil moisture, salt, and nutrient contents. The accumulative contribution rate of soil moisture and salt contents in the first principal component accounted for 35.70%, and that of soil nutrient content in the second principal component reached 25.97%. There were 4 types of habitats for the plant community distribution, i. e., fenny--light salt--medium nutrient, moist--medium salt--medium nutrient, mesophytic--medium salt--low nutrient, and medium xerophytic-heavy salt--low nutrient. Along these habitats, swamp vegetation, meadow vegetation, riparian sparse forest, halophytic desert, and salinized shrub were distributed. In the wetlands and surrounding lands of mid- and lower reaches of Tarim River, the ecological dominance of the plant communities was markedly and unitary-linearly correlated with the compound gradient of soil moisture and salt contents. The relationships between species diversity, ecological dominance, and compound gradient of soil moisture and salt contents were significantly accorded to binary-linear regression model.

Biodiversity↗

A 3D canted antiferromagnetic porous metal-organic framework with anatase topology through assembly of an analogue of polyoxometalate.

The unique porous metal-organic framework {KCo3(C6H4O7)(C6H5O7)(H2O)2.8H2O}8 (1), which exhibits an unprecedented infinite 3D (3,6)-connected decorated anatase net, has been obtained by hydrothermal reaction. Upon dehydration, the compound retains crystallinity and exhibits a type I N2 sorption isotherm, characteristic of a microporous solid with apparent Langmuir surface area 939 m2/g and pore volume 0.31 cm3/g. Magnetic measurements for both 1 and dehydrated 1 show the spin-canted antiferromagnetic state below 5 K and a magnetic hysteresis loop at 2 K. Thus, dehydrated 1 represents the first metal-organic framework for which microporosity and a spin-canted antiferromagnetic state coexist, which demonstrates that the self-assembly of organo-polymetal clusters and metal ions can provide a potential route to magnetic porous metal-organic frameworks.

Journal Article↗

Antioxidant intake and risk of osteoporotic hip fracture in Utah: an effect modified by smoking status.

The role of antioxidant intake in osteoporotic hip fracture risk is uncertain and may be modified by smoking. In the Utah Study of Nutrition and Bone Health, a statewide, population-based case-control study, the authors investigated whether antioxidant intake was associated with risk of osteoporotic hip fracture and whether this association was modified by smoking status. The analyses included data on 1,215 male and female cases aged > or = 50 years who incurred a hip fracture during 1997-2001 and 1,349 age- and sex-matched controls. Diet was assessed by food frequency questionnaire. Among ever smokers, participants in the highest quintile of vitamin E intake (vs. the lowest) had a lower risk of hip fracture after adjustment for confounders (odds ratio = 0.29, 95% confidence interval (CI): 0.16, 0.52; p-trend < 0.0001). The corresponding odds ratio for beta-carotene intake was 0.39 (95% CI: 0.23, 0.68; p-trend = 0.0004), and for selenium intake it was 0.27 (95% CI: 0.12, 0.58; p-trend = 0.0003). Vitamin C intake did not have a significant graded association with hip fracture risk among ever smokers. Similar findings were obtained when an overall antioxidant intake score was used (odds ratio = 0.19, 95% CI: 0.10, 0.37; p-trend < 0.0001). No similar associations were found in never smokers. Antioxidant intake was associated with reduced risk of osteoporotic hip fracture in these elderly subjects, and the effect was strongly modified by smoking status.

Aged↗

Coeloglossum viride var. bracteatum extract attenuates D-galactose and NaNO2 induced memory impairment in mice.

The aim is to study the neuroprotective effects of CE, a special extract from Coeloglossum viride (L.) Hartm. var. bracteatum (Willd.), on memory deficits in senescent mice induced by consecutive injection of d-galactose and NaNO(2) for 60 days. Oral administration of CE (2.5 mg kg(-1), 5 mg kg(-1)) started from 47th day of the experiment. Water maze test was used to evaluate the learning and memory function of mice. The contents of MDA and GSH and the activities of SOD and GSH-px in brain tissue were determined using different biochemical methods. The alterations in hippocampus morphology were assessed. Immunoreactive cells of Tau-2 and NT-3 in the hippocampus were counted by immunohistochemical staining. The results indicated that combined injection of d-galactose and NaNO(2) induced memory impairment of mice. In addition, SOD and GSH-px activities and GSH level decreased while MDA level increased in mouse brain. Tau-2 positive neurons increased while NT-3 positive neurons decreased remarkably in the hippocampus. Administration of CE for 14 days significantly improved the cognitive deficits and the biochemical markers mentioned above and reduced the histological lesions in mouse brain. These results suggest that CE is worth testing for further preclinical study aimed for senescence and dementia.

Animals↗

ATM regulates target switching to escalating doses of radiation in the intestines.

Although stem cells succumbing to reproductive death are assumed to be the single relevant targets in radiation tissue damage, recent studies showed intestinal stem cell damage is conditionally linked to crypt endothelial apoptosis, defining a two-target model. Here we report that when mouse intestines were protected against microvascular apoptosis, radiation switched as the dose escalated to a previously unrecognized crypt stem cell target, activating ceramide synthase-mediated apoptosis to initiate intestinal damage. Whereas ataxia telangiectasia-mutated (ATM) kinase normally represses ceramide synthase, its derepression in Atm(-/-) mice increased crypt stem cell radiosensitivity 3.7-fold without sensitizing the microvascular response. Discovery of this intestinal radiosensitivity mechanism allowed design of an antisense Atm oligonucleotide treatment which phenocopied the Atm(-/-) mouse, reordering ceramide synthase-mediated stem cell death to become the first-line gastrointestinal response of wild-type littermates. These experiments indicate that tissues operate multiple potential targets activated consecutively according to their inherent radiosensitivities that may be reordered therapeutically to control radiation tissue responses.

Animals↗

Caspase-dependent and -independent activation of acid sphingomyelinase signaling.

Recent evidence suggests clustering of plasma membrane rafts into ceramide-enriched platforms serves as a transmembrane signaling mechanism for a subset of cell surface receptors and environmental stresses (Grassme, H., Jekle, A., Riehle, A., Schwarz, H., Berger, J., Sandhoff, K., Kolesnick, R., and Gulbins, E. (2001) J. Biol. Chem. 276, 20589-20596; Cremesti, A., Paris, F., Grassme, H., Holler, N., Tschopp, J., Fuks, Z., Gulbins, E., and Kolesnick, R. (2001) J. Biol. Chem. 276, 23954-23961). Translocation of the secretory form of acid sphingomyelinase (ASMase) into microscopic rafts generates therein the ceramide that drives raft coalescence. This process serves to feed forward Fas activation, with approximately 2% of full caspase 8 activation sufficient for maximal ASMase translocation, leading to death-inducing signaling complex formation within ceramide-rich platforms, and apoptosis. Here we report that treatment of Jurkat T cells with UV-C also induces ASMase translocation into rafts within 1 min, catalyzing sphingomyelin hydrolysis to ceramide and raft clustering. In contrast to Fas, UV-induced ASMase translocation and activation were caspase-independent. Nonetheless, ceramide-rich platforms promoted UV-C-induced death signaling, because ASMase inhibition or raft disruption inhibited apoptosis, improving clonogenic cell survival. These studies thus define two distinct mechanisms for biologically relevant ASMase activation within rafts; a Fas-mediated mechanism dependent upon caspase 8 and FADD, and a UV-induced mechanism independent of caspase activation. Consistent with this notion, genetic depletion or pharmacologic inhibition of caspase 8 or FADD, which render Jurkat cells incapable of sphingolipid signaling and apoptosis upon Fas ligation, did not impair these events upon UV-C stimulation.

Amino Acid Chloromethyl Ketones↗

Animal fat consumption and pancreatic cancer incidence: evidence of interaction with cigarette smoking.

PURPOSE: A large difference in fat intake and pancreatic cancer incidence exists among populations worldwide. This study investigated the relation between fat consumption and pancreatic cancer risk at the population level. METHODS: Fat consumption data for nine periods (1964-1994) and age-standardized pancreatic cancer incidence data for five periods (1973-1997) in 35 countries were derived from the Food and Agriculture Organization and World Health Organization, respectively. RESULTS: A significant positive correlation was found between animal fat consumption and pancreatic cancer incidence in all periods examined (r=0.40-0.74, p=0.021 to < 0.0001 in men and r=0.50-0.66, p=0.01 to 0.0001 in women). After adjustment for smoking and other confounders, animal fat consumption in all nine periods considered was still significantly and positively associated with pancreatic cancer incidence in the 1993 to 1997 period in both sexes. The stratified analysis showed that this association was significant only in countries with below median level of smoking (< 2273 cigarettes/adult/year). A similar but less pronounced effect was observed for total fat consumption. CONCLUSIONS: The consumption of fat, especially animal fat, was associated with an increased risk of pancreatic cancer and this association was modified by levels of cigarette smoking.

Animals↗

Effect of diphenyl dimethyl bicarboxylate on concanavalin A-induced liver injury in mice.

Diphenyl dimethyl bicarboxylate (DDB) is a hepatoprotectant and used in the treatment of chronic viral hepatitis patients in China. The aim of the present paper was to investigate the effect of DDB on liver injury mediated by immune response in concanavalin A (Con A)-treated mice. A dose of Con A 30 mg/kg was injected via the tailvein to induce liver injury in mice. Serum alanine transaminase (ALT), aspartate aminotransferase (AST), total bile acid (TBA), total bilirubin (TBIL) and tumor necrosis factor alpha (TNF-alpha) level as well as liver TNF-alpha mRNA expression were determined. The following results were obtained: (1) Prior oral administration of DDB 150 mg/kg markedly reduced the elevated serum ALT, TBA and TBIL levels, and the liver lesions in Con A-treated mice; (2) DDB significantly inhibited the elevation of serum TNF-alpha and liver TNF-alpha mRNA expression 2 h after Con A injection; (3) DDB significantly inhibited hepatocyte nuclear DNA fragmentation 12 h after Con A injection; (4) DDB dose-dependently prevented the direct DNA damage induced by CuSO(4)-Phen-Vit C-H(2)O(2) system in vitro, and the ex vivo experiment also showed that the administration of DDB reduced the susceptibility of mouse liver nuclei DNA to CuSO(4)-Phen-Vit C-H(2)O(2) system. These results suggest that DDB could directly protect hepatocyte DNA from oxidative damage, and inhibit TNF-alpha mRNA expression in liver tissue, which resulted in prevention of liver damage induced by Con A in mice.

Adjuvants, Immunologic↗

Milk consumption in relation to incidence of prostate, breast, colon, and rectal cancers: is there an independent effect?

Milk contains a wide variety of ingredients, such as nutrients, hormones, and chemical contaminants. Whether milk consumption is associated with the risk of prostate, breast, colon, and rectal cancers is unclear and was evaluated in this study. Data on milk consumption for 9 time periods (1964-1994) and incidence rates of prostate, female breast, colon, and rectal cancers, mostly around 1993-1997, in 38 countries were obtained from the Food and Agriculture Organization and World Health Organization, respectively. Milk consumption was strongly correlated with incidence rates of prostate cancer (r = 0.65-0.69; all P < 0.0001) and breast cancer (r = 0.64-0.74; all P < 0.0001) in all the nine time periods examined. A modest positive correlation was found for colon and rectal cancers in both sexes (all P < 0.05, except for rectal cancer in the first three time periods). The previous findings remained essentially unchanged after adjustment for vegetable, alcohol, and cigarette consumption but disappeared after further adjustment for non-milk fat consumption, except for breast cancer in the last three time periods. The present study does not support an overall substantial effect of milk consumption on the risk of prostate, breast, colon, and rectal cancers at the population level.

Animals↗

Effects of novel anxiolytic 4-butyl-alpha-agarofuran on levels of monoamine neurotransmitters in rats.

4-butyl-alpha-agarofuran (AF-5) is a new compound derived from alpha-agarofuran, a constituent extracted from Aquillaria agallocha Roxb. Our previous research has shown that AF-5 has significant antianxiety activity in several animal models. In this study, an antianxiety effect was observed in a social interaction test after acute treatment with AF-5 (0.5-4.0 mg/kg, i.p.) in rats. Using high-performance liquid chromatography (HPLC)-electrochemical detection (ECD), we further investigated the effects of AF-5 on monoamine neurotransmitters both in rat brain tissues and in striatum dialysates. After acute administration of AF-5 (5.0 mg/kg, i.p.), serotonin (5-hydroxytryptamine, 5-HT) tissue levels significantly decreased by 26.3%, 30.4%, and 17.4% of the vehicle-control levels, in the striatum, cortex, and midbrain, respectively. The dopamine level decreased by 34.7% in the striatum and 19.0% in the midbrain, while in the hypothalamus, it increased to 156.6%. The epinephrine level decreased by 34.6% in the cortex. In cerebral microdialysis perfusates from rat striatum, the extracellular dopamine level declined stepwise after treatment with AF-5 (10.0 mg/kg, i.p.). By 200 min postinjection, the dopamine level reached a minimum, about 40% of the baseline value. At the same time, the extracellular levels of 5-hydroxyindolacetic acid, 3-4-dihydroxyphenylacetic acid, and homovanillic acid increased significantly, the maximum values were 150%, 145%, and 175% above baseline, respectively. This study suggests that AF-5 is a potent anxiolytic agent, and that its beneficial action may be related to its effects on central monoamine neurotransmitters.

Animals↗