TY - JOUR
T1 - Highly sensitive and selective anticancer effect by conjugated HA-cisplatin in non-small cell lung cancer overexpressed with CD44
AU - Quan, Yu Hua
AU - Kim, Byungji
AU - Park, Ji Ho
AU - Choi, Yeonho
AU - Choi, Young Ho
AU - Kim, Hyun Koo
N1 - Funding Information:
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MEST) (no.: 2012012166). Address correspondence to Hyun Koo Kim, Department of Thoracic and Cardiovascular Surgery, Korea University College of Medicine, Seoul 152–703, Korea. E-mail: kimhyunkoo@korea.ac.kr and Yeonho Choi, Department of Biomedical Engineering, Korea University, Seoul 136–703, Korea. E-mail: yeonhochoi@korea.ac.kr
Publisher Copyright:
© 2014 Informa Healthcare USA, Inc.
PY - 2014/12/1
Y1 - 2014/12/1
N2 - In spite of severe side effects, chemotherapy is widely used as a major anticancer treatment in non-small cell lung cancer (NSCLC). In order to enhance the therapeutic properties and reduce side effects, enormous efforts have been devoted to direct anticancer agents specifically to tumor tissues by the use of nanoparticles, or cancer cell marker attached drugs. However, cell-specific chemotherapy is still in its infancy and is not applicable to all types of cancers due to the complexity of the cancer occurrence and progress. In this study, we demonstrate that hyaluronan (HA)-conjugated cisplatin has highly selective and sensitive anticancer effects in NSCLC cells that overexpress the trans-membrane receptor, CD44, as HA is a specific ligand for CD44. In proliferation experiments, HA-conjugated cisplatin showed dramatic cell viability decreases (from 100% to 42.31%) in H1299 cells, which overexpress CD44, whereas no such change was observed in A549 and HFL1, which have little to no expression of CD44. More importantly, conjugation with HA decreased the dosage concentration of cisplatin by 50-fold for both cytotoxic and anti-metastatic effects. In addition, HA-cisplatin conjugate treatment selectively decreased migration (from 100% to 7.8%) and invasiveness (from 100% to 21.4%, respectively) of H1299. Based on our experimental results, we strongly believe that HA-cisplatin conjugate is a potential anticancer chemo-agent, which target CD44 overexpression in NSCLC, with minimal side effects and high therapeutic properties.
AB - In spite of severe side effects, chemotherapy is widely used as a major anticancer treatment in non-small cell lung cancer (NSCLC). In order to enhance the therapeutic properties and reduce side effects, enormous efforts have been devoted to direct anticancer agents specifically to tumor tissues by the use of nanoparticles, or cancer cell marker attached drugs. However, cell-specific chemotherapy is still in its infancy and is not applicable to all types of cancers due to the complexity of the cancer occurrence and progress. In this study, we demonstrate that hyaluronan (HA)-conjugated cisplatin has highly selective and sensitive anticancer effects in NSCLC cells that overexpress the trans-membrane receptor, CD44, as HA is a specific ligand for CD44. In proliferation experiments, HA-conjugated cisplatin showed dramatic cell viability decreases (from 100% to 42.31%) in H1299 cells, which overexpress CD44, whereas no such change was observed in A549 and HFL1, which have little to no expression of CD44. More importantly, conjugation with HA decreased the dosage concentration of cisplatin by 50-fold for both cytotoxic and anti-metastatic effects. In addition, HA-cisplatin conjugate treatment selectively decreased migration (from 100% to 7.8%) and invasiveness (from 100% to 21.4%, respectively) of H1299. Based on our experimental results, we strongly believe that HA-cisplatin conjugate is a potential anticancer chemo-agent, which target CD44 overexpression in NSCLC, with minimal side effects and high therapeutic properties.
KW - CD44
KW - Hyaluronan-cisplatin conjugate
KW - Lung cancer
UR - http://www.scopus.com/inward/record.url?scp=84908597322&partnerID=8YFLogxK
U2 - 10.3109/01902148.2014.905656
DO - 10.3109/01902148.2014.905656
M3 - Article
C2 - 25299431
AN - SCOPUS:84908597322
SN - 0190-2148
VL - 40
SP - 475
EP - 484
JO - Experimental Lung Research
JF - Experimental Lung Research
IS - 10
ER -