Klf activation following growth factor inhibition in human cancer.

We measured total gene expression in the primary tumors of humans treated with the vascular endothelial growth factor alpha (VEGF-A) inhibitor bevacizumab (Avastin) to describe the tumor transcriptional landscape in response to growth factor restriction and to identify genes that mediate the compensatory, feedback responses that define the general growth factor inhibition resistance gene signature. We report here activation of the Kruppel-lke factor KLF4 in the primary tumors of humans treated bevacizumab. Pluripotency and embryonic growth factor requirements are mechanistically linked here in the primary transcriptional response to VEGF-A inhibition in vivo.

Authors

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-10-31
DOI
https://doi.org/10.5281/zenodo.23837145
Primary Topic
Kruppel-like factors research
Type
preprint
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preprint

Klf activation following growth factor inhibition in human cancer.

Shahan Mamoor
Zenodo (CERN European Organization for Nuclear Research)
Kruppel-like factors research
preprint

Klf activation following growth factor inhibition in human cancer.

Shahan Mamoor
preprint en

Abstract

We measured total gene expression in the primary tumors of humans treated with the vascular endothelial growth factor alpha (VEGF-A) inhibitor bevacizumab (Avastin) to describe the tumor transcriptional landscape in response to growth factor restriction and to identify genes that mediate the compensatory, feedback responses that define the general growth factor inhibition resistance gene signature. We report here activation of the Kruppel-lke factor KLF4 in the primary tumors of humans treated bevacizumab. Pluripotency and embryonic growth factor requirements are mechanistically linked here in the primary transcriptional response to VEGF-A inhibition in vivo.

Zenodo (CERN European Organization for Nuclear Research)
Kruppel-like factors research
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