Ewing sarcoma tumors can be split into two groups for targeted care

Ewing sarcoma tumors can be split into two groups for targeted care
A. Bright field images of CCH1 and CCH2 cells B. CCH1 and CCH2 cells cells stained with antibody towards CD99 (green) and DAPI (blue) C. Western blots on CCH1 and CCH2 cell lysates probed with the indicated antibodies, confirming differences in EphA2 phosphorylation between CCH1 and CCH2. D. Immunofluorescence imaging of IGF1R-stained CCH1 and CCH2 cells starved, treated with IGF1 or treated with Linsitinib for 2 hours. Individual channels are shown below the merged images. Nuclear IGF1R in CCH1 cells does not change localization with either treatment. IGF1 treatment induces slight internalization of IGF1R in CCH2 cells and this is inhibited by Linsitinib. Credit: Clinical Cancer Research (2022). DOI: 10.1158/1078-0432.CCR-22-2587

Ewing sarcoma is a fast-growing form of bone and soft tissue cancer that strikes about 200 children and young adults per year in the United States.

Caught early, before the tumors have spread, the five-year survival rate for this cancer reaches 70-80%. However, over 25% of patients with initially localized disease and a much higher percentage of patients with initially metastatic disease have a relapse. Treatments have proven much less effective against metastatic or relapsed disease.

Now, a study led by experts at Cincinnati Children's helps reveal why treatment outcomes can vary among patients and even in the same patient over the course of disease. Detailed findings were published in Clinical Cancer Research.

The research team, led by corresponding author Rashmi Hegde, Ph.D., Division of Developmental Biology, reports finding two subgroups of Ewing sarcoma that respond differently to targeted . The team also shows that both groups can occur in the same person as disease progresses, suggesting that repeated biopsies may be needed over time to assure the most accurate treatment targeting.

Receptor location matters

Rapid cell growth in many types of cancer depends heavily on the insulin-like growth factor-1 receptor (IGF-1R) cell signaling pathway. But in Ewing sarcoma, tumors respond differently to drugs intended to block that pathway based on whether receptors are located in, or on, the cancer cell.

In one group of tumors, the Cincinnati Children's team found these critical receptors concentrated within tumor cell nuclei, where IGF-1R promoted tolerance to DNA damage and made the less vulnerable to treatment. But in another group, the receptors were located primarily in outer cell membranes, the tumor were under high levels of replication stress, and were more susceptible to treatment with the experimental compound Linsitinib.

In mouse studies, and in lab tests involving , the team did find a way to shrink tumors with nuclear IGF-1R. It required a combination of Linsitinib and another experimental drug called AZD1775. That second drug, part of a class of drugs known as checkpoint inhibitors, disrupts the function of the WEE1 protein, which helps regulate the timing of cell division.

"While the combined treatment approach shrank tumors from both groups of Ewing sarcoma tumors, the higher cost and potential for with combination therapies suggest that the two-drug approach may be of greater benefit to patients with nuclear IGF-1R containing tumors," Hegde says.

Next step: Refining biomarkers

Using current technology, care teams could conduct multiple biopsies over the course of disease management to determine the best course of treatment. But biopsies can be painful and come with risks. Less-invasive testing methods would be preferred.

"That means more research is needed to establish biomarkers that can be collected from blood or other less-invasive ways and still accurately distinguish between these classes of Ewing sarcoma tumors," Hegde says.

More information: Upendra K. Soni et al, Molecularly defined subsets of Ewing Sarcoma tumors differ in their responses to IGF1R and WEE1 inhibition, Clinical Cancer Research (2022). DOI: 10.1158/1078-0432.CCR-22-2587

Journal information: Clinical Cancer Research
Citation: Ewing sarcoma tumors can be split into two groups for targeted care (2022, November 17) retrieved 24 April 2024 from https://medicalxpress.com/news/2022-11-ewing-sarcoma-tumors-groups.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Explore further

Biological pathways found that drive genomic changes and bone metastasis in ewing sarcoma, a rare childhood cancer


Feedback to editors