Amino acid transport system L is differently expressed in human normal oral keratinocytes and human oral cancer cells

التفاصيل البيبلوغرافية
العنوان: Amino acid transport system L is differently expressed in human normal oral keratinocytes and human oral cancer cells
المؤلفون: Seoul Lee, Heung-Joong Kim, Do Kyung Kim, Chong Heon Lee, Bong Kyu Choi, Hyun Kuk Kim, Jung Hoon Yoon, Yoshikatsu Kanai, Sang Gun Ahn, In Jin Kim, Hitoshi Endou, Moon Jin Jeong, Kyu Yong Jung, Jong-Keun Kim, Soo Ah Kim
المصدر: Cancer Letters. 222:237-245
بيانات النشر: Elsevier BV, 2005.
سنة النشر: 2005
مصطلحات موضوعية: Keratinocytes, chemistry.chemical_classification, Cancer Research, System L, Gene Expression Profiling, Protein subunit, Carcinoma, Transporter, Biology, Polymerase Chain Reaction, Amino acid, Gene expression profiling, Oncology, Biochemistry, chemistry, Epidermoid carcinoma, Amino Acid Transport System L, Cancer cell, Humans, Mouth Neoplasms, Amino acid transporter
الوصف: Previously, we reported the expression and function of system L amino acid transporter in KB human oral epidermoid carcinoma cells. In the present study, therefore, we investigated the expression and function of system L amino acid transporter in human normal oral keratinocytes (HNOK) and compared the expressions and functions of system L amino acid transporters in HNOK and KB cells. The HNOK expressed L-type amino acid transporter 1 (LAT1) and L-type amino acid transporter 2 (LAT2) with their subunit 4F2hc in the plasma membrane but the expression of LAT1 was very weak, which is in contrast to the KB cells expressing LAT1 but not LAT2 with the 4F2hc in the plasma membrane. The [14C] L-leucine uptake by HNOK, as well as KB cells, was inhibited by the system L selective inhibitor BCH. The majority of [14C] L-leucine uptake was, therefore, mainly mediated by LAT2 in the HNOK and by LAT1 in the KB cells. These results suggest that the transport of neutral amino acids including several essential amino acids into the HNOK and KB cells are mainly mediated by LAT2 and LAT1, respectively. The specific inhibition of LAT1 in oral cancer cells could be a new rationale for anti-cancer therapy.
تدمد: 0304-3835
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d3ae8549a53792f3bc2d32d25f640c9Test
https://doi.org/10.1016/j.canlet.2004.09.040Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....7d3ae8549a53792f3bc2d32d25f640c9
قاعدة البيانات: OpenAIRE