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Manzoor, A.

Publications and source records attributed to Manzoor, A..

3 recordsLinked to original sources

XAI-ecDNA: A Proof-of-Concept Framework for Explainable Multi-Modal Extrachromosomal DNA Detection Using Synthetic FISH and Genomics

Extrachromosomal DNA (ecDNA) is a key contributor to aggressive tumor evolution and drug resistance across multiple cancer types. Yet detection methods suffer from limited performance and lack interpretability. Moreover, paired fluorescence in situ hybridization (FISH) and genomic datasets necessary for developing multi-modal artificial intelligence tools remain unavailable in public repositories. We developed an explainable multi-modal framework combining genomic copy number profiles from 500 samples (TCGA, CytoCellDB) with synthetic FISH images generated via StyleGAN2-ADA trained on 247 published images. The framework employs early fusion of ResNet-50 image features and multi-layer perceptron processed genomic data through gated attention. A Biological Rationale Score (BRS) provides SHAP-based explanations with stability quantification and uncertainty estimates. Expert cytogeneticists validated synthetic image biological plausibility. Twelve clinical experts evaluated predictions in a crossover study. On synthetic images, our framework achieved AUROC 0.87, significantly outperforming genomic-only (0.72), image-only (0.79), and late fusion (0.84) baselines (all p<0.001). BRS identified MYC amplification (76% of cases), nuclear morphology (68%), and spatial clustering (56%) as top predictive features, aligning with known biology. Explanation stability reached Kendalls {tau}=0.74. Expert diagnostic confidence improved by 0.9 points (Cohens d=1.26, p<0.001) with explanations. Model calibration was excellent (ECE=0.042). This proof-of-concept demonstrates multi-modal explainable ecDNA detection potential. However, all results are on synthetic images; validation with real clinical FISH data is essential before deployment. The methodology provides a transparent template for interpretable AI development in data-scarce medical domains.

genomics↗

Mdm2 restrains the activity of the CRL4Cdt2 E3 ubiquitin ligase to promote cell cycle progression through the G2/M phase

The canonical function of the Mdm2 oncoprotein is widely recognized as the negative regulation of the p53 tumor suppressor. However, growing evidence indicates that its physiological activities extend far beyond p53. Here, we show that Mdm2 promotes cell cycle progression at the G2/M phase through the ubiquitin-mediated degradation of the substrate recognition adaptor Cdt2 of the CRL4Cdt2 E3 ubiquitin ligase complex, independently of p53. The attenuation of CRL4Cdt2 activity by Mdm2 stabilizes its cell cycle-specific substrates including p21, Set8, and Cdt1, at the G2/M phase following their proteasomal degradation in the S phase. Furthermore, the delay in cell cycle progression at the G2/M phase and the decreased cell proliferation observed in the absence of Mdm2 are largely caused by an increase in Cdt2 and a subsequent decrease in p21. Collectively, our data illustrate a previously unexplored mechanism by which Mdm2 regulates the cell cycle and promotes cellular proliferation by neutralising the CR4Cdt2 E3 ubiquitin ligase activity and subsequently stabilizing p21.

molecular biology↗

Bacteriophages can be used as infection control agents: A proof-of concept study involving anti-Acinetobacter baumannii phage

Hospital acquired infections are responsible for morbidity and mortality worldwide. Acinetobacter spp. infections are particularly notorious for complicating patient management in ICU settings. Extremely high mortality rates are associated with Acinetobacter infections because of their resistance to first- and second-line drugs. There is imminent need to develop infections control systems that are specific and environment friendly. Here, we report a proof-of-concept anti-Acinetobacter spp. bacteriophage-based infection control assay that is very target specific as well as innocuous to environment. extensively drug resistant (XDR) Acinetobacter baumannii strain was inoculated at various solid surfaces. A bacteriophage, enriched in the same strain, was applied on the inoculated surfaces. Phenol (carbolic acid) was used as a positive control. We show that bacteriophages can be used as infection control agents. In our assay, they killed XDR Acinetobacter baumannii present on solid surfaces. Our bacteriophage was extremely effective at reducing the CFU of inoculated strain to almost undetectable levels.

microbiology↗