Scientists at Hokkaido University have identified how inflammatory changes in tumors caused by chemotherapy trigger blood vessel anomalies and thus drug-resistance, resulting in poor prognosis of cancer patients.

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New study findings could help devise treatment strategies like development of inhibitors targeting ABCB1 and IL-8, to suppress drug resistance and improve prognosis.
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However, several years ago, the group's mice experiments showed TEC can obtain various anomalies, suggesting blood vessels, as well as cancer cells, can contribute to making tumors drug-resistant.
For example, the group demonstrated for the first time that TEC in blood vessels resist paclitaxel - a chemotherapy medication used for second-line treatment of urothelial cancer - due to the expression of ABCB1 which pumps out the drug from blood vessels.
However, much remains unknown about how human blood vessels are involved in cancer acquiring drug-resistance.
To help unravel this mystery, the group first analyzed tumor tissue samples from urothelial cancer patients before and after they underwent first-line chemotherapy.
In addition, they analyzed TEC in blood vessels and bladder cancer cells to study how chemotherapy affects ABCB1 expression. The results showed that the increased secretion of interleukin-8 (IL-8) in cancer cells after chemotherapy caused inflammatory changes, increasing the ABCB1 expression in TEC.
"Our study provides evidence, for the first time in humans, that inflammatory changes in tumors can cause drug resistance in cancer blood vessels," says Kyoko Hida of Hokkaido University who led the group. "These findings could help devise new treatment strategies, such as the development of inhibitors targeting ABCB1 and IL-8, to suppress drug resistance and improve prognosis."
Source-Eurekalert
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