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<p>As neuroendocrine neoplasms (NEN) undergo increasing dedifferentiation, CXC chemokine receptor type 4 (CXCR4) becomes upregulated. Higher levels of CXCR4 are associated with invasive growth, metastasis formation, and poor prognosis. CXCR4 is considered a potential diagnostic biomarker and a promising target for precision therapies — e.g., endoradiotherapeutic approaches, monoclonal antibodies, or small-molecule inhibitors. A variety of systemic therapies are used to treat metastatic NEN, which may modulate CXCR4 expression and potentially influence the efficacy of future CXCR4-targeted strategies. In the NEN cell lines BON-1, QGP-1, and MS-18, we applied cisplatin, etoposide, streptozotocin, 5-fluorouracil, temozolomide, and everolimus- all systemic agents used in highly proliferative NEN. Following incubation, CXCR4 expression was quantified by qRT-PCR, Western blot, and immunohistochemistry. The functional receptor activity was determined by measuring uptake of the radioligand [68Ga]Pentixafor. Cisplatin induced a significant reduction in CXCR4 mRNA levels in BON-1 and QGP-1 cells (<i>p</i> &lt; 0.05) and decreased radioligand uptake in QGP-1 and MS-18. Etoposide, 5-FU, and streptozotocin had no significant impact on CXCR4 expression or uptake activity. Temozolomide and Everolimus markedly diminished both CXCR4 mRNA and protein levels with no significant impact on radioligand uptake. In high-grade NEN cell lines, Cisplatin, Everolimus, and Temozolomide substantially diminish CXCR4 expression, with Cisplatin significantly decreasing CXCR4-targeted radioligand uptake. These findings might have an impact on the optimal therapy sequence and patient selection for future CXCR4-targeted approaches. Further, the decreased CXCR4 expression could represent a new mechanism of action of the established drugs Cisplatin, Temozolomide, and Everolimus.</p>

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Impact of neuroendocrine neoplasm-specific systemic treatments on expression and function of CXCR4 in neuroendocrine tumor cells

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年1月31日

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  • Christof Däubler,
  • Clara Böttcher,
  • Laura-Sophie Landwehr,
  • Alexander Meining,
  • K. Michalski,
  • F. Reiter,
  • Rudolf A. Werner,
  • Philipp Hartrampf,
  • Dorothee Rogoll,
  • Alexander Weich

摘要

As neuroendocrine neoplasms (NEN) undergo increasing dedifferentiation, CXC chemokine receptor type 4 (CXCR4) becomes upregulated. Higher levels of CXCR4 are associated with invasive growth, metastasis formation, and poor prognosis. CXCR4 is considered a potential diagnostic biomarker and a promising target for precision therapies — e.g., endoradiotherapeutic approaches, monoclonal antibodies, or small-molecule inhibitors. A variety of systemic therapies are used to treat metastatic NEN, which may modulate CXCR4 expression and potentially influence the efficacy of future CXCR4-targeted strategies. In the NEN cell lines BON-1, QGP-1, and MS-18, we applied cisplatin, etoposide, streptozotocin, 5-fluorouracil, temozolomide, and everolimus- all systemic agents used in highly proliferative NEN. Following incubation, CXCR4 expression was quantified by qRT-PCR, Western blot, and immunohistochemistry. The functional receptor activity was determined by measuring uptake of the radioligand [68Ga]Pentixafor. Cisplatin induced a significant reduction in CXCR4 mRNA levels in BON-1 and QGP-1 cells (p < 0.05) and decreased radioligand uptake in QGP-1 and MS-18. Etoposide, 5-FU, and streptozotocin had no significant impact on CXCR4 expression or uptake activity. Temozolomide and Everolimus markedly diminished both CXCR4 mRNA and protein levels with no significant impact on radioligand uptake. In high-grade NEN cell lines, Cisplatin, Everolimus, and Temozolomide substantially diminish CXCR4 expression, with Cisplatin significantly decreasing CXCR4-targeted radioligand uptake. These findings might have an impact on the optimal therapy sequence and patient selection for future CXCR4-targeted approaches. Further, the decreased CXCR4 expression could represent a new mechanism of action of the established drugs Cisplatin, Temozolomide, and Everolimus.