Review Article

[Retracted] Long Noncoding RNAs: New Regulators of Resistance to Systemic Therapies for Gastric Cancer

Table 2

lncRNAs associated with drug resistance in the treatment of GC.

lncRNAsLocationExpressionDrugsMechanismReferences

AK022798UpregulatedCisplatinNotch 1 can promote the lncRNA AK022798 expression and result in the formation of SGC7901/cisplatin and BGC823/cisplatin cells.[133]
BCAR4 (breast cancer anti-estrogen resistance 4)16p13.13UpregulatedCisplatinOverexpression of BCAR4 in SGC7901 cells increased resistance to cisplatin, while reduced BCAR4 expression increased the sensitivity of SGC7901/cisplatin cells to cisplatin.[134]
CASC2 (cancer susceptibility 2)10q26.11DownregulatedCisplatinCASC2 overexpression overcame cisplatin resistance in gastric cancer by sponging miR-19a.[135]
CASC9 (cancer susceptibility 9)8q21.13UpregulatedPaclitaxel, adriamycinCASC9 knockdown restored chemosensitivity to paclitaxel and adriamycin by decreasing the expression of MDR1protein.[136]
GHET1 (gastric carcinoma proliferation enhancing transcript 1)7q36.1UpregulatedCisplatinHighly expressing GHET1 promoted the development of MDR, which was related to the Bax, Bcl-2, MDR1, and MRP1 gene expression in gastric cancer cells.[137]
LEIGCDownregulated5-FluorouracilOverexpression of LEIGC suppressed tumor growth and cell proliferation and enhanced the sensitivity of gastric cancer cells to 5-fluorouracil, whereas knockdown of LEIGC showed the opposite effect.[138]
MALAT1 (metastasis-associated lung adenocarcinoma transcript 1)11q13.1UpregulatedVincristine, cisplatinMALAT1 acts as a competing endogenous RNA for miR-23b-3p and attenuates the inhibitory effect of miR-23b-3p on ATG12, leading to chemo-induced autophagy and chemoresistance in GC cells.[139]
MRUL (also named DMTF1, cyclin D-binding myb-like transcription factor 1)7q21.12UpregulatedMDRMRUL depletion reduced ABCB1 mRNA levels in a dose- and time-dependent manner, and ABCB1 was responsible for drug transporters.[140]
PTV1 (polytropic virus 1)UpregulatedCisplatinOverexpression of lncRNA PVT1 in gastric carcinoma promotes the development of MDR.[141]
XLOC_006753UpregulatedMDRHigh expression of XLOC_006753 promoted the development of MDR, which was activated by the PI3K/AKT/mTOR pathway in GC cells.[142]
ZFAS (zinc finger antisense)Chromosome 8UpregulatedCisplatin, paclitaxelThe silencing of ZFAS1 inhibited the growth, proliferation, cell cycle progress, migration, invasion, EMT, and chemotherapeutic tolerance by blocking the Wnt/β-catenin signaling in gastric cancer cells.[143]