Publications by authors named "Mulong Du"

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  • A study analyzed 26,544 single nucleotide polymorphisms (SNPs) in 291 FRGs and identified 661 SNPs linked to overall survival (OS) in NSCLC patients, later validating these findings in a separate patient group.
  • Two SNPs, FER rs7716388 A>G and SULF1 rs11785839 G>C, were found to be significantly associated with improved survival rates, suggesting that these genetic variants could serve as progn
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  • * This study analyzed tissue samples to identify gene modules associated with the progression from normal cervix to cervical intraepithelial neoplasia and ultimately CC, using advanced techniques like transcriptome sequencing and machine learning models.
  • * Findings revealed CARMN as a significant gene in CC, showing that reduced CARMN expression affects key cellular pathways, leading to an increased risk of CC, with specific genetic variants also linked to this risk.
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Background: PANoptosis is a cell death pathway involved in pyroptosis, apoptosis and necrosis, and plays a key role in the development of malignant tumors. However, the molecular signature of PANoptosis in colorectal cancer (CRC) prognosis has not been thoroughly explored. The present study aimed to develop a novel prognostic model based on PANoptosis-related genes in CRC.

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  • T cell exhaustion is linked to decreased effectiveness of immune checkpoint inhibitors in lung cancer, which has the highest mortality rate among cancers, although the genetic variants related to T cell exhaustion in non-small cell lung cancer (NSCLC) prognosis are not well studied.!* -
  • A two-stage analysis using existing genome-wide association study (GWAS) datasets identified 1,721 single nucleotide polymorphisms (SNPs) related to T cell exhaustion that were associated with overall survival in NSCLC patients, with 125 confirmed significant after further validation.!* -
  • Three specific SNPs (rs10493829, rs2239193, and rs3136651) showed a significant association with overall survival, highlighting that certain genotypes
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  • A previous study identified the WWOX gene as a risk factor for developing acute lymphoblastic leukemia (ALL), leading to deeper genetic analysis of the disease using a sample of 269 cases and 1039 controls from Chinese descent.
  • The analysis revealed that the serotonin-activated cation-selective channel complex gene-set plays a significant role in ALL, with the T allele of rs33940208 linked to a lower risk of developing the disease, and the A allele of rs6779545 associated with a higher risk.
  • Combining these genetic variants showed that having multiple risk alleles significantly increases the likelihood of developing childhood ALL, highlighting the need for further research to understand the molecular mechanisms involved and improve prevention strategies.
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Ferroptosis, a form of regulated cell death, is characterized by iron-dependent lipid peroxidation. It is recognized increasingly for its pivotal role in both cancer development and the response to cancer treatments. We assessed associations between 370,027 single-nucleotide polymorphisms (SNPs) within 467 ferroptosis-related genes and survival of non-small cell lung cancer (NSCLC) patients.

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  • Metabolic dysfunction-associated fatty liver disease (MAFLD) is a rising cause of chronic liver disease globally, prompting the need for dietary intervention strategies.
  • A panel of 55 international experts conducted a study to reach a consensus on dietary modifications for preventing MAFLD, covering various aspects from epidemiology to management.
  • Recommended strategies include following a balanced diet, increasing whole grains and plant-based foods, and reducing red meat and processed foods, along with advocating for physical activity and possibly maintaining Mediterranean or DASH diets.
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  • Cigarette smoking directly increases mutation burden in bladder cancer, specifically affecting driver mutations like RB1, which sees a twofold increase in mutation rates among smokers under 65 years.
  • The study utilized various genomic databases and experiments to analyze how these mutations influence tumor growth and the immune environment in bladder cancer patients.
  • Findings indicate that RB1 mutations hinder the cytochrome P450 pathway and alter immune cell interactions, potentially enhancing cancer development linked to smoking.
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  • B cells are important in cancer progression, particularly non-small cell lung cancer (NSCLC), but the impact of genetic variants in immunity-related genes on patient survival is unclear.
  • The study analyzed over 10,000 genetic variants in B cell-related genes among nearly 1,200 NSCLC patients and identified 369 single nucleotide polymorphisms (SNPs) linked to overall survival, further validating 18 SNPs in an additional patient group.
  • Two specific SNPs were found to significantly influence patient survival, with certain unfavorable combinations of these genotypes leading to poorer outcomes, and gene expression analyses indicated that specific alleles correlate with higher gene activity in lung tissues.
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Smooth muscle cells in major arteries play a crucial role in regulating coronary artery disease. Conversion of smooth muscle cells into other adverse cell types in the artery propels the pathogenesis of the disease. Curtailing artery plaque buildup by modulating smooth muscle cell reprograming presents us a new opportunity to thwart coronary artery disease.

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  • Hypoxia plays a significant role in cancer aggression, impacting processes like blood vessel formation and immune response, yet the influence of genetic variants in hypoxia-related genes on survival in non-small cell lung cancer (NSCLC) remains unclear.
  • Researchers studied 16,092 single-nucleotide polymorphisms (SNPs) in 182 hypoxia-related genes among NSCLC patients, using data from two cancer studies to identify any survival associations.
  • They found that the ERRFI1 gene variant rs28624 was linked to lower overall survival rates in patients, indicating that certain genetic variations could affect how long individuals with NSCLC live, possibly by influencing gene expression.
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  • The study investigates the role of PIWI-interacting RNAs (piRNAs) and their genetic variants in the risk and progression of prostate cancer (PCa) using data from over 85,000 PCa cases and 166,000 controls.
  • A specific genetic variant, rs17201241, is linked to increased expression of PROPER, a piRNA associated with higher risk and severity of PCa, which works by affecting mRNA interactions and promoting cancer progression through the p38 MAPK signaling pathway.
  • Targeting PROPER has shown potential in suppressing tumor growth in experimental models, suggesting it could be a valuable target for new PCa treatments.
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Mitochondrial DNA (mtDNA) has emerged as a pivotal component in understanding the etiology and susceptibility of cancer. A recent study by Chen and colleagues delineated the germline genetic effect of mtDNA single-nucleotide polymorphisms (SNP) and haplogroups across pan-cancer risk. They identified a subset of mtSNPs and the corresponding risk score, as well as haplogroups A and M7 alongside their genetic interactions, conferring a protective effect against various cancers.

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  • The gene C1GALT1 is linked to gastric cancer, with specific genetic variant rs35999583 G>C shown to potentially influence cancer risk based on a study using genetic data.
  • Higher C1GALT1 mRNA levels were found in gastric tumors compared to normal tissues, linked to poorer patient survival rates.
  • The research suggests that variations in C1GALT1 could serve as a predictor for gastric cancer risk and may also relate to immune cell activity in the tumor environment.
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  • - The research highlights that left and right colon cancers have unique clinical and molecular traits influenced by their specific tumor environments and cancer cell characteristics.
  • - By analyzing over 426,000 single cells from colon cancer patients, two distinct gene expression patterns were identified for left- and right-sided tumors.
  • - Left-sided cancers show a strong focus on cell growth and metabolism, while right-sided cancers are linked to immune evasion mechanisms, particularly in smokers, revealing how these tumors interact with their surroundings.
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Tobacco carcinogens metabolism-related genes (TCMGs) could generate reactive metabolites of tobacco carcinogens, which subsequently contributed to multiple diseases. However, the association between genetic variants in TCMGs and bladder cancer susceptibility remains unclear. In this study, we derived TCMGs from metabolic pathways of polycyclic aromatic hydrocarbons and tobacco-specific nitrosamines, and then explored genetic associations between TCMGs and bladder cancer risk in two populations: a Chinese population of 580 cases and 1101 controls, and a European population of 5930 cases and 5468 controls, along with interaction and joint analyses.

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  • Early-onset prostate cancer (EOPC), which affects men aged 55 or younger, presents a significant genetic risk and shows potential for early detection but typically results in poor prognoses.
  • A study involving over 167,000 male participants aimed to develop age-specific polygenic risk scores (PRS) for personalized risk assessment and found that EOPC-PRS was strongly linked to EOPC risk compared to late-onset cases.
  • The research highlighted that EOPC is more influenced by genetic factors like family history, while late-onset prostate cancer (LOPC) is more associated with environmental and lifestyle factors.
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Background: Individual exposure to environmental pollutants, as one of the most influential drivers of respiratory disorders, has received considerable attention due to its preventability and controllability. Considering that the extracellular vesicle (EV) was an emerging intercellular communication medium, recent studies have highlighted the crucial role of environmental pollutants derived EVs (EPE-EVs) in respiratory disorders.

Methods: PubMed and Web of Science were searched from January 2018 to December 2023 for publications with key words of environmental pollutants, respiratory disorders and EVs.

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The development of an effective survival prediction tool is key for reducing colorectal cancer mortality. Here, we apply a three-stage study to devise a polygenic prognostic score (PPS) for stratifying colorectal cancer overall survival. Leveraging two cohorts of 3703 patients, we first perform a genome-wide survival association analysis to develop eight candidate PPSs.

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Tobacco carcinogens are recognized as critical hazard factors for bladder tumorigenesis, affecting the prognosis of patients through aromatic amines components. However, the specific function of tobacco carcinogens and systematic assessment models in the prognosis of bladder cancer remains poorly elucidated. We retrieved bladder cancer specific tobacco carcinogens-related genes from Comparative Toxicogenomic Database, our Nanjing Bladder Cancer cohort and TCGA database.

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Background: Screening reduces colorectal cancer (CRC) burden by allowing early resection of precancerous and cancerous lesions. An adequate selection of high-risk individuals and a high uptake rate for colonoscopy screening are critical to identifying people more likely to benefit from screening and allocating healthcare resources properly. We evaluated whether combining a questionnaire-based interview for risk factors with fecal immunochemical test (FIT) outcomes for high-risk assessment is more efficient and economical than a questionnaire-based interview-only strategy.

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