Transcriptome analysis indicates TFEB1 and YEATS4 as regulatory transcription factors for drug resistance of ovarian cancer

被引:17
作者
Kim, Yi Rang [1 ]
Park, Mi Sung [2 ]
Eum, Ki Hwan [3 ,4 ]
Kim, Juhee [3 ,4 ]
Lee, Jeong Won [5 ,6 ]
Bae, Taejeong [7 ]
Lee, Dae Ho [8 ]
Choi, Jin Woo [3 ,4 ,9 ]
机构
[1] Yuseong Sun Hosp, Dept Hematooncol, Daejeon, South Korea
[2] Wonkwang Univ, Inst Metab Dis, Sch Med, Iksan, Jeonbuk, South Korea
[3] Wonkwang Univ, Sch Dent, Wonkwang Inst Interfused Biomed Sci, Iksan, Chonbuk, South Korea
[4] Wonkwang Univ, Sch Dent, Dent Res Inst, Iksan, Chonbuk, South Korea
[5] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Obstet & Gynecol, Seoul, South Korea
[6] Sungkyunkwan Univ, Sch Med, Samsung Biomed Res Inst, Seoul, South Korea
[7] Mayo Clin, Dept Hlth Sci Res, Div Biomed Stat & Informat, Rochester, MN USA
[8] Wonkwang Univ, Sch Med & Hosp, Dept Internal Med, Iksan, Jeonbuk, South Korea
[9] Seoul Natl Univ, Adv Inst Convergence Technol, Suwon, Gyeonggi Do, South Korea
关键词
cancer; transcription factor; drug resistance; bioinformatics; THERAPEUTIC TARGET; EXPRESSION; PATHWAY; BIOGENESIS; CISPLATIN; NETWORK; FAMILY; GAS41;
D O I
10.18632/oncotarget.5208
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ovarian cancer is an intractable disease because patients with ovarian cancer frequently develop drug resistance after long-term chemotherapy. Despite the availability of cumulative information on drug-resistant patients, strategies to reverse drug resistance have still not been established. In this study, we analyzed drug resistance-associated transcription factors (TFs) in ovarian cancer. Gene expression profiles of 15 drug-resistant and 11 drug-sensitive patients with ovarian cancer were compared. Our results showed that TFs TFEB1 and YEATS4 regulated the expression of downstream target genes. These 2 TFs have already been implicated in tumorigenesis or metastasis. To our knowledge, this is the first study to evaluate the involvement of these TFs in drug resistance of ovarian cancer. Interestingly, 70% knockdown of each of these TFs with siRNAs resulted in approximately 20%similar to 30% recovery of drug sensitivity. Further, combination treatment of ovarian cancer cells with TFEB1 and YEATS4 siRNAs resulted in 35% reversal of drug resistance. The effect of these TFs on chemoresistance seemed to be associated with intrinsic apoptosis-related pathways, such as p53 activation, and not with the suppression of drug transport. Thus, we suggest a novel approach to reverse chemoresistance of ovarian cancer by suppressing TFEB1 and YEATS4.
引用
收藏
页码:31030 / 31038
页数:9
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