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Active Targeting of Versatile Nanocomplex Using the Novel Biomarker of Breast Cancer Stem Cells.
Koh, Eun-Young; Kim, Keun-Sik; Park, Hee-Bin; Kim, Jong-Seok; Kim, Pyung-Hwan.
Affiliation
  • Koh EY; Department of Biomedical Laboratory Science, Konyang University, Daejeon 35365, Republic of Korea.
  • Kim KS; Department of Biomedical Laboratory Science, Konyang University, Daejeon 35365, Republic of Korea.
  • Park HB; Department of Biomedical Laboratory Science, Konyang University, Daejeon 35365, Republic of Korea.
  • Kim JS; Myunggok Medical Research Institute, College of Medicine, Konyang University, Daejeon 35365, Republic of Korea.
  • Kim PH; Department of Biomedical Laboratory Science, Konyang University, Daejeon 35365, Republic of Korea.
Int J Mol Sci ; 24(1)2022 Dec 30.
Article in En | MEDLINE | ID: mdl-36614128
ABSTRACT
Breast cancer in women is one of the most common life-threatening malignancies. Despite of the development for the improved treatment, there are still many limitations to overcome. Among them, cancer stem cells (CSCs) are well known for tumor formation, development, cellular heterogeneity, and cancer recurrence. Therefore, to completely cure breast cancer, treatment of both cancer and CSC is required. To selectively target CSCs, we generated a liposome-based smart nano complex using CEACAM 6 (CD66c) antibody (Ab), a novel cell-surface biomarker of breast-derived CSCs (BCSCs) discovered in our previous research. Selective and increased cellular uptake was observed in BCSCs treated with CD66c Ab-conjugated rhodamine-labeled liposomes (CDRHOL) depending on the expression level of CD66c. CD66c Ab-conjugated doxorubicin (DOX)-loaded liposomes (CDDOXL) selectively showed increased cell killing effects in BCSCs with high CD66c expression levels. In an in vivo animal study, CDRHOL showed enhanced accumulation in xenografted BCSC tumors with low delivery into non-target organs. Moreover, mice treated with CDDOXL have assessed the decreased induction ability of immune response by low expression levels of pro-inflammatory cytokines and reduced liver toxicity by histopathological analysis. Finally, the improved antitumor effect of CDDOXL was evaluated in a metastatic BCSC mouse model via systemic administration. Collectively, our study is the first to demonstrate that a multi-functional nano complex using a novel surface biomarker of BCSC may be a more effective therapeutic agent for the treatment of cancer and CSCs.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Liposomes / Neoplasm Recurrence, Local Limits: Animals Language: En Journal: Int J Mol Sci Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Liposomes / Neoplasm Recurrence, Local Limits: Animals Language: En Journal: Int J Mol Sci Year: 2022 Document type: Article