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Inhibition of bone and muscle metastases of lung cancer cells by a decrease in the number of monocytes/macrophages

Title: Inhibition of bone and muscle metastases of lung cancer cells by a decrease in the number of monocytes/macrophages
Authors: Hiraoka, Koji; Zenmyo, Michihisa; Watari, Kousuke; Iguchi, Haruo; Fotovati, Abbas; Kimura, Yusuke N.; Hosoi, Fumihito; Shoda, Takanori; Nagata, Kensei; Osada, Hiroyuki; Ono, Mayumi; Kuwano, Michihiko
Source: Cancer Science ; volume 99, issue 8, page 1595-1602 ; ISSN 1347-9032 1349-7006
Publisher Information: Wiley
Publication Year: 2008
Collection: Wiley Online Library (Open Access Articles via Crossref)
Description: Attention has recently focused on the critical role of inflammatory responses in the tumor stroma that provide favorable conditions for cancer‐cell growth and invasion/metastasis. In particular, macrophages recruited into the tumor stroma and activated, known as tumor‐associated macrophages, are suggested to promote tumorigenesis. In this study, we examined the effect of a decrease in the number of monocytes/macrophages in peripheral blood and the tumor stroma on the development of bone and muscle metastases by lung cancer cells. Treatment with clodronate encapsulated by liposomes (Cl 2 MDP‐LIP) has been developed for the depletion of monocytes/macrophages in an animal model. Subcutaneous administration of Cl 2 MDP‐LIP markedly reduced the number of monocytes in peripheral blood, resulting in efficient suppression of both bone metastasis and muscle metastasis when lung cancer HARA‐B cells were injected into the left cardiac ventricle of mice. Treatment with Cl 2 MDP‐LIP significantly reduced the number of macrophages in tumors and the number of osteoclasts in bone marrow, as well as peripheral monocytes in mice harboring lung cancer cells. In contrast, treatment with an osteoclast‐targeting antibiotic, reveromycin A, inhibited bone metastasis by lung cancer cells, but not muscle metastasis. The survival of human macrophages in culture was found to be specifically blocked by Cl 2 MDP‐LIP, but not by reveromycin A. Cl 2 MDP‐LIP thus exerted antimetastatic effects in both bone and muscle whereas reveromycin A did so only in bone. Liposome‐encapsulated bisphosphonate may modulate metastasis through decreasing the number of monocytes/macrophages in both peripheral blood and the tumor stroma, suggesting that tumor‐associated macrophages might be suitable targets for antimetastatic therapy. ( Cancer Sci 2008; 99: 1595–1602)
Document Type: article in journal/newspaper
Language: English
DOI: 10.1111/j.1349-7006.2008.00880.x
Availability: https://doi.org/10.1111/j.1349-7006.2008.00880.x; https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1349-7006.2008.00880.x; https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1349-7006.2008.00880.x
Rights: http://onlinelibrary.wiley.com/termsAndConditions#vor
Accession Number: edsbas.8BAD63B5
Database: BASE