Publications by authors named "A van de Kuil"

Article Synopsis
  • BTK inhibitors have improved outcomes for mantle cell lymphoma (MCL) patients, but the disease remains incurable due to resistance issues.
  • Research indicates that HCK, a Src-family tyrosine kinase, is linked to poor prognosis in MCL and its inhibition can limit cell growth and adhesion.
  • The dual inhibitor KIN-8194 effectively targets both BTK and HCK, showing strong anti-growth effects on MCL cells regardless of their resistance to existing BTK inhibitors, suggesting its potential as a new treatment option.
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We studied the prognostic value of primary tumor sidedness in metastatic colorectal cancer over time and across treatment lines. Population data on synchronous metastatic colorectal cancer patients were extracted from the Netherlands Cancer Registry and SEER database. Pubmed, EMBASE and Cochrane library were searched for prospective studies on metastatic colorectal cancer to conduct a meta-analysis.

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Objectives: Location of the primary tumor has prognostic value and predicts the effect of certain therapeutics in synchronous metastatic colorectal cancer. We investigated whether the association between primary tumor resection (PTR) and overall survival (OS) also depends on tumor location.

Methods: Data on synchronous metastatic colorectal cancer patients from the Netherlands Cancer Registry (n=16,106) and Surveillance, Epidemiology, and End Results (SEER) registry (n=19,584) were extracted.

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Background: The survival and proliferation of multiple myeloma (MM) cells in the bone marrow (BM) critically depend on interaction with stromal cells expressing the chemokine CXCL12. CXCL12 regulates the homing to the BM niche by mediating the transendothelial migration and adhesion/retention of the MM cells. The gamma isoform of CXCL12 (CXCL12γ) has been reported to be highly expressed in mouse BM and to show enhanced biological activity compared to the 'common' CXCL12α isoform, mediated by its unique extended C-terminal domain, which binds heparan sulfate proteoglycans (HSPGs) with an extraordinary high affinity.

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