AI Article Synopsis

  • Renal cell carcinoma (RCC) is a deadly and diverse group of cancers that share a common origin but exhibit different characteristics and behaviors; accurate diagnosis is crucial.
  • To improve the standardization of immunohistochemistry (IHC) testing for RCC subtypes, a study utilized a specific monoclonal antibody (clone WT49) to analyze the expression of the WT1 protein in 56 adult cases, marking the largest research focused solely on adult RCC.
  • The study found that 12.5% of cases tested positive for WT1, primarily in clear cell RCC, and highlighted the need for further investigation and standardization in WT1 expression to enhance future targeted immunotherapy for RCC.

Article Abstract

Renal cell carcinoma (RCC) is arguably the deadliest form of genitourinary malignancy and is nowadays viewed as a heterogeneous series of cancers, with the same origin but fundamentally different metabolisms and clinical behaviors. Immunohistochemistry (IHC) is increasingly necessary for RCC subtyping and definitive diagnosis. is a complex gene involved in carcinogenesis. To address reporting heterogeneity and WT1 IHC standardization, we used a recent N-terminus targeted monoclonal antibody (clone WT49) to evaluate WT1 protein expression in 56 adult RCC (aRCC) cases. This is the largest WT1 IHC investigation focusing exclusively on aRCCs and the first report on clone WT49 staining in aRCCs. We found seven (12.5%) positive cases, all clear cell RCCs, showing exclusively nuclear staining for WT1. We did not disregard cytoplasmic staining in any of the negative cases. Extratumoral fibroblasts, connecting tubules and intratumoral endothelial cells showed the same exclusively nuclear WT1 staining pattern. We reviewed WT1 expression patterns in aRCCs and the possible explanatory underlying metabolomics. For now, WT1 protein expression in aRCCs is insufficiently investigated, with significant discrepancies in the little data reported. Emerging WT1-targeted RCC immunotherapy will require adequate case selection and sustained efforts to standardize the quantification of tumor-associated antigens for aRCC and its many subtypes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026801PMC
http://dx.doi.org/10.3390/biomedicines10040912DOI Listing

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