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Author Spotlight: Unveiling the Role of TMOD3 in Platinum Resistance and Immune Infiltration in Ovarian Cancer
Published on: August 2, 2024
Organic cation transporter 6 directly confers resistance to anticancer platinum drugs
Tetsuya Oguri1, Eiji Kunii1, Satoshi Fukuda1
1Department of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Abstract:
Organic cation transporters (OCTs) of the solute carrier family 22 have a critical role in the cellular uptake of anticancer platinum drugs. Recently, we found that a decreased OCT6 expression is associated with a reduced intracellular uptake of cisplatin (CDDP), and concomitant resistance to CDDP. In the present study, we examined whether OCTs directly confer resistance to another platinum drug, oxaliplatin (L-OHP). To address this, we used parental lung cancer cell lines, PC-14 and SBC3; L-OHP-resistant sublines, PC-14/L-OHP and SBC3/L-OHP; and one CDDP-resistant subline PC-14/CDDP, to examine the relationships between the expression of OCTs and intracellular platinum drug concentration or platinum drug resistance. The two L-OHP-resistant sublines showed cross resistance to CDDP and L-OHP, and a decreased expression of OCT6. The intracellular accumulation of L-OHP in PC-14/L-OHP cells was reduced compared with the parental cells. The findings suggested that a reduced OCT6 expression confers platinum drug resistance in the sublines by decreasing the uptake of platinum drugs. Using the PC-14/CDDP cell line engineered to overexpress OCT6, we confirmed that the intracellular L-OHP concentration was increased concomitantly with OCT6 overexpression compared with the parental cell line. Additionally, OCT6 was expressed in a screening panel of lung and colon cancer tissues and matched normal control tissues. Taken together with the previous results, the present findings indicate that OCT6 is directly involved in platinum drug resistance by mediating platinum drug uptake in cancer cells.
Insights
Organic cation transporter 6 (OCT6) significantly impacts platinum-based chemotherapy. Reduced OCT6 expression lowers drug uptake, causing resistance to cisplatin and oxaliplatin in cancer cells.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Organic cation transporters (OCTs) are crucial for platinum-based anticancer drug uptake.
- Previous research linked decreased OCT6 expression to cisplatin resistance.
- The role of OCTs in oxaliplatin resistance remained unclear.
Purpose of the Study:
- To investigate if OCTs directly confer resistance to oxaliplatin.
- To examine the relationship between OCT expression, platinum drug concentration, and resistance.
- To determine OCT6's role in mediating platinum drug uptake in cancer.
Main Methods:
- Utilized parental and oxaliplatin-resistant lung cancer cell lines (PC-14, SBC3).
- Assessed OCT expression levels in resistant and parental cell lines.
- Measured intracellular concentrations of oxaliplatin and cisplatin.
- Examined OCT6 expression in clinical cancer tissues.
Main Results:
- Oxaliplatin-resistant cell lines exhibited cross-resistance to cisplatin and reduced OCT6 expression.
- Intracellular oxaliplatin accumulation was lower in resistant cells.
- Overexpression of OCT6 in cisplatin-resistant cells increased intracellular oxaliplatin levels.
- OCT6 was detected in clinical lung and colon cancer tissues.
Conclusions:
- Reduced OCT6 expression contributes to platinum drug resistance by decreasing drug uptake.
- OCT6 plays a direct role in mediating platinum drug uptake and resistance in cancer cells.
- OCT6 is a potential therapeutic target for overcoming platinum resistance.
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