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Data · dataset · 2026

Supplementary Figure 2 from The H63D Polymorphism in the <i>HFE</i> Gene Promotes Aggressive Disease Phenotypes in Pancreatic Ductal Adenocarcinoma

Listed in ZivaHub and Deakin Research Online and DMU Figshare — shown once because both records carry DOI 10.1158/1078-0432.34041296

<p>(A) Representative immunohistochemical staining for Ki67 performed on FFPE human PDAC specimens from wild-type/non-carrier patients (WT, <i>n</i> = 57) and H63D carriers (<i>n</i> = 25) and (B) quantification of Ki67-positive area.

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(C) Representative Western blot analysis of HFE protein expression in FFPE PDAC tissues from WT patients and H63D carriers (including both heterozygous and homozygous cases). (D) Densitometric quantification of HFE band intensity.

Values are presented as median ±SD. (E) Distribution of loss of heterozygosity (LOH) fractions at the <i>HFE</i> locus (chromosome 6) across PDAC samples. LOH was calculated using germline-informative heterozygous sites and matched tumor sequencing data, integrating genotype calls and allele-specific read counts.

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The distribution is strongly skewed toward low values, with most samples showing minimal or no allelic imbalance. Mean (dashed red line) and median (dotted green line) LOH fractions are indicated. These data indicate that LOH at the <i>HFE</i> locus is infrequent and not recurrent in PDAC.</p>

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Inferred from text
Disease 75% · Oncology and carcinogenesis 73% · Sequencing 75%
Provenance · 3 source records, 19 field assertions
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