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Jiazhang Wei

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Open access Aug 2026

Mendelian randomization analysis of the causal relationship between allergic rhinitis and depression and underlying mediation mechanisms

Background Epidemiological studies have documented an association between allergic rhinitis (AR) and depression (DE), but causal interpretation is limited by confounding and reverse causation. We applied bidirectional two-sample Mendelian randomization to assess the direction and magnitude of this association and to explore candidate pathways. Methods Summary-level data were obtained separately from 2 AR GWAS (Study AR1: n = 112 583; Study AR2: n = 83 529) and 2 DE GWAS (Study DE1: n = 484 598; Study DE2: n = 462 933) of European ancestry. Independent single-nucleotide polymorphisms (P < 5 × 10−8; LD r2 < 0.001) served as instruments. Forward and reverse estimates were derived using inverse-variance weighted MR, with MR-Egger and weighted median analyses for sensitivity. A two-step framework estimated separate indirect effects through sleep duration (SD) and anxiety symptoms (ANX). Multivariable MR simultaneously modeled AR and 8 additional traits—dynamic activity ratio, light-intensity physical activity, moderate-to-vigorous activity, loneliness (LON), neuroticism (NEU), immunoglobulin E (IgE), interleukin-6, and fasting insulin—to estimate conditional effects. Pleiotropy and heterogeneity were assessed using MR-Egger intercepts, Cochran’s Q and MR-PRESSO. Results Across 2 AR instrument sets and 2 depression outcomes, genetic liability to AR was consistently associated with a small increase in depression risk (IVW ORs 1.0105–1.0125), whereas reverse-direction analyses provided no evidence that depression liability increased AR risk. AR liability was nominally associated with sleep duration (β = 0.079; 95% CI 0.005–0.153; P = 0.036) and anxiety symptoms (β = 0.031; 95% CI 0.004–0.058; P = 0.025), and was more strongly associated with total IgE (β = 1.981; 95% CI 1.200–2.762; P = 6.60 × 10−7). The separate indirect effects through sleep duration (β = 0.005; 95% CI −0.021 to 0.031; descriptive proportion 47.7%) and anxiety (β = 0.003; 95% CI −0.012 to 0.018; descriptive proportion 24.2%) were imprecise and were not combined. In MVMR, loneliness showed the strongest positive conditional association with depression (OR = 1.243; 95% CI 1.165–1.325; P = 3.40 × 10−11), whereas the conditional AR and IgE estimates were null. Because conditional instrument strength was unavailable, MVMR findings were interpreted as supportive pathway evidence. Conclusions Genetic liability to AR was consistently associated with a small increase in depression risk across 4 dataset pairings. Although the magnitude alone is insufficient to support individual-level clinical decision-making, the concordant findings add etiological evidence for an AR–depression relationship. Sleep duration and anxiety remain plausible but unconfirmed candidate pathways, while the MVMR findings prioritize loneliness for further validation. Total IgE was more consistent with an AR-related biomarker than an independent mediator.

Shao-Jie Zhang, Rong Wang, Jing-Jin Weng et al. · 0 citations
Aug 2026

Frequent mutations in the BIRC3 gene promote metastatic potential of nasopharyngeal carcinoma cells through the TRAF2-NF-κB pathway.

Nasopharyngeal carcinoma (NPC) is a head and neck cancer characterized by highly locoregionally invasive behavior attributable to the latent infection with Epstein-Barr virus (EBV) and genomic instability. It is well established that EBV-encoded oncogenic molecules actively contribute to the malignant behavior of NPC cells. However, the mechanism by which aberrant genomic alterations enable NPC cells to become aggressive remains largely unknown. In the present study, whole-exome sequencing (WES) revealed that the gene encoding the baculoviral IAP repeat-containing 3 (BIRC3) protein was frequently mutated in circulating tumor cells (CTCs) but not in paired primary tumor cells from patients with metastatic NPC. A minigene assay indicated that the c.637 A > G mutation disrupted normal mRNA splicing, resulting in the partial deletion of Exons 2 and 3 and altered stability of BIRC3 mRNA. In vitro experiments demonstrated that ectopic expression of the BIRC3c.637A>G mutant enhanced NPC cell invasive properties, including proliferation, resistance to apoptosis, migration, and invasion. Furthermore, overexpression of wild-type BIRC3 promoted invasive characteristics in NPC cells through the TRAF2-NF-κB signaling axis. In summary, BIRC3 acts as a regulator of the malignant features of NPC cells. Frequent BIRC3 mutations in CTCs, such as the c.637 A > G mutation, further enhance the metastatic potential of disseminated NPC cells by inducing aberrant alternative splicing. These findings suggest the therapeutic feasibility of targeting the BIRC3/TRAF2/NF-κB axis in the treatment of NPC.

Xue Liu, Yuping Liu, Bi-Yun Zhu et al. · 0 citations
Review Open access Aug 2026

Adaptive epithelial-mesenchymal bi-directional transition: A key invasive plasticity for tumor metastasis

The pivotal role of EMP in tumor metastasis and treatment resistance is elucidated and the clinical translational potential of targeting EMP-related signaling pathways as a personalized anti-metastasis therapeutic strategy is discussed.

Yuping Liu, Lihong Huang, Yujuan Huang et al. · 0 citations

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