8P - Organic cation transporter 6 directly confers resistance to anticancer platinum drugs

Date 19 December 2015
Event ESMO Asia 2015 Congress
Session Poster presentation 1
Topics Cancer biology
Basic Scientific Principles
Presenter Tetsuya Oguri
Citation Annals of Oncology (2015) 26 (suppl_9): 1-7. 10.1093/annonc/mdv517
Authors T. Oguri, E. Kunii, S. Fukuda, T. Uemura, O. Takakuwa, K. Maeno, Y. Kanemitsu, H. Ohkubo, M. Takemura, Y. Ito, A. Niimi
  • Department Of Respiratory Medicine, Allergy And Clinical Immunology, Nagoya City University, 467-8601 - Nagoya/JP

Abstract

Aim/Background

Organic cation transporters (OCTs) of the solute carrier family 22 have been identified as uptake transporters for the charge state of a substrate such as cationic drugs. The OCTs have an isoform of OCT1, OCT2, OCT3, and OCT6. Each OCT has a characteristic pattern of tissue expression and transport-specific substrates, and plays an important role in the cellular accumulation of antucancer platinum drugs. Previously we found that decreased OCT6 expression is associated with the resistance to cisplatin (CDDP) by decreased intracellular uptake of CDDP. In this study we examined whether OCT6 directly confers resistance to another platinum drug oxaliplatin (L-OHP).

Methods

We used lung cancer cell line PC-14, and SBC3 cells, and established the L-OHP-resistant lung cancer subline PC-14/L-OHP and SBC3/LOHP cells. Further we used a forced expression of OCT6 cells by a transfection an OCT6 gene SLC22A16 using a forced expression vector. We examined the expression of OCTs in relation with intracellular platinum drug concentration or platinum drug resistance using these cells.

Results

Both L-OHP resistant sublines showed cross resistance to CDDP and L-OHP, and decreased expression of OCT6. The intracellular accumulation of L-OHP in PC-14/LOHP cells was reduced compared to their parental cells. These findings suggest that OCT6 expression confers platinum drug resistance in the sublines by enhancing the decreased uptake of platinum drugs into cancer cells. Further, we confirmed that intracellular L-OHP concentration are increased concomitant with decreased resistance to L-OHP in OCT6 overexpressed cells.

Conclusions

Taken together with our previous results, the present findings indicate that alteration of OCT6 expression is directly involved in platinum drug resistance according to platinum drug uptake into cancer cells.

Clinical trial identification

Disclosure

All authors have declared no conflicts of interest.