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The origins of seven types of kidney cancer, including several rare subtypes, have been identified by researchers at the Wellcome Sanger Institute, Great Ormond Street Hospital (GOSH), the Princess Máxima Center for Pediatric Oncology and Oncode Institute. The findings confirm that these cancers have their origin in specific forms of developmental cells present in the maturing fetus.

The study, amoxicillin dosage for kids published today (23 June) in Nature Communications, used computational methods to analyze existing datasets and pinpoint the ‘cellular signals’ given off by different cancers as they emerge. This method holds promise as a tool for diagnosing patients with rare cancers—in the study, one patient’s cryptic kidney cancer was identified as a Wilms-like tumor by looking at its cellular signals.

All cancers are derived from normal cells that have started to multiply uncontrollably. By comparing patterns of gene expression in cancer and normal cells, it is possible to learn about aspects of each tumor’s origin and behavior. This type of analysis has been made possible by the advent of single-cell mRNA sequencing, a high-resolution technology that can identify different cell types present in a tissue according to the genes expressed by individual cells.

Previous studies have used these techniques to compare normal and diseased tissue in some of the most common kidney cancers, but to conduct single-cell sequencing on many hundreds of tumors would not be achievable.

In this study, researchers at the Wellcome Sanger Institute and their collaborators turned to computational techniques to mine Human Cell Atlas (HCA) reference data and databases of tumor gene expression. They assessed mRNA signals in 1,300 childhood and adult renal tumors, spanning seven different tumor types, in order to investigate the origins of these cancers.

The results confirmed that these childhood cancers are developmental in origin, occurring after errors in a particular developmental cell type’s journey to maturity. In contrast, adult kidney cancers emerged from mature cell types and do not revert to a developmental pattern of gene expression in the vast majority of cases.

Each cancer type was also found to exhibit unique ‘cellular signals’, or patterns of gene expression, that could be used to classify them in future.

Dr. Matthew Young, first author of the study from the Wellcome Sanger Institute, said: “It has long been assumed that childhood tumors have ‘fetal’ origins. Now we can replace that loose definition with a precise, quantitative measurement of the cellular signals that different tumor types exhibit. Our analysis also refutes the theory that adult tumors revert to a developmental state, unless they are a highly lethal subtype of adult kidney cancer.”

The study sheds light on the behavior and origins of some kidney tumor subtypes whose rarity would have made it difficult to examine otherwise. These were congenital mesoblastic nephroma, clear cell sarcoma of the kidney, malignant rhabdoid tumor of the kidney, and chromophobe renal cell carcinoma.

The method pioneered in the study also helped to classify one patient’s tumor, which clinicians had been unable to diagnose fully.

Dr. Karin Straathof, a senior author of the study from Great Ormond Street Hospital, said: “Sometimes it is not possible to fully diagnose childhood kidney cancers via the usual methods, which can impact our ability to adopt the best course of treatment. One of the samples used in this study was from a child with one of these undiagnosed tumors. But by analyzing the genes expressed by the tumor cells, we were able to recognize it as Wilms’ tumor. My hope is that this approach can be used in such cases in future.”

In recent studies, researchers have identified the origins of individual childhood cancers, such as neuroblastoma, using mRNA single-cell sequencing on small numbers of tumors. Here, computational analysis of existing data has been used to determine the origin of a larger groups of childhood cancers.

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