Tumor targeting with docosahexaenoic acid-conjugated docetaxel for inhibiting lung cancer metastasis to bone.

Oncol Lett

Key Laboratory of Forest Plant Ecology, Ministry of Education, Northeast Forestry University, Harbin, Heilongjiang 150040, P.R. China.

Published: September 2018

AI Article Synopsis

  • Docetaxel (DTX) is a common treatment for lung cancer but is less effective for patients with bone metastasis due to its nonspecific nature.
  • The study created a new compound, DTX-DHA, by combining DTX with docosahexaenoic acid (DHA), aimed at improving the inhibition of lung cancer metastasis to bone.
  • DTX-DHA showed similar effectiveness to DTX while increasing the maximum tolerated dose and extending the mean survival time of treated patients, suggesting it may offer a better therapeutic approach for lung cancer metastasis to bone.

Article Abstract

Docetaxel (DTX) is currently used as a first- or second-line drug treatment for patients with lung cancer, however, it is less effective for the treatment of patients with bone metastasis of lung cancer. This is primarily due to the fact that docetaxel is nonspecific. In the present study, docosahexaenoic acid (DHA) was selected as a tumor-targeting ligand, and DHA-conjugated DTX (DTX-DHA) was prepared for inhibiting lung cancer metastasis to bone. The anti-cancer activity assay revealed that DTX-DHA exhibited a similar antitumor efficacy to DTX . The maximum tolerated dose of DTX-DHA was increased compared with that of DTX. The present study results indicated that DTX-DHA exhibited an improved inhibition efficacy of lung cancer metastasis to bone in comparison with DTX . Encouragingly, the mean survival time of the DTX-DHA group (30.60 days) was increased compared with the DTX group (26.10 days; P<0.01). Furthermore, the results of cell migration and osteoclast-induced formation assays suggested that DTX-DHA inhibited lung cancer metastasis to bone primarily by affecting lung cancer cell migration. These results indicate that DTX-DHA may exhibit a potential therapeutic effect against lung cancer metastasis to bone.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096075PMC
http://dx.doi.org/10.3892/ol.2018.9047DOI Listing

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