AI Article Synopsis

  • This study explores how removing the spleen (splenectomy) affects the growth of lung cancer in mice, particularly how it interacts with radiation treatment.
  • Human and mouse lung cancer cells were injected into different strains of mice, and the researchers analyzed the impact of splenectomy and radiation on tumor growth and immune responses.
  • The findings indicate that splenectomy can hinder tumor growth but does not enhance radiation's effects; however, it alters immune cell activity and improves outcomes when combined with anti-PD-1 therapy.

Article Abstract

Purpose: This study aims to investigate the effect of splenectomy on radiation-mediated growth inhibition and immune modulation in lung cancer xenograft models.

Materials And Methods: Human non-small cell lung cancer H1299 cells and murine Lewis lung carcinoma LL/2-luc cells were injected into the right hind leg of BALB/c-nude mice and C57BL/6 mice, respectively. Splenectomy or sham operation was performed prior to tumor cell injection or before and after irradiation during tumor growth. Irradiation was delivered with 2-3 fractions of 6 Gy X-ray using a linear accelerator. Flow cytometry analysis was performed for immune cell profiling.

Results: Splenectomy prior to tumor injection or at early stage inhibited growth of LL/2-luc tumors but not that of H1299 tumors; however, it did not enhance the antitumor effect of radiation regardless of intervention timing. Flow cytometry analysis showed monocytic myeloid-derived suppressor cells (MDSCs) and activated CD8+ T cells increased after irradiation in the tumors of splenectomized mice, compared to those of sham-operated mice. Administration of anti-PD-1 (programmed death-1) antibodies improved the ability of splenectomy to attenuate the growth of irradiated tumors.

Conclusion: Splenectomy has paradoxical effects on radiation-induced tumor growth inhibition, depending on tumor types and intervention timing, but it has an immune-modulating effect when combined with radiation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984136PMC
http://dx.doi.org/10.3857/roj.2021.00885DOI Listing

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