Background
Paclitaxel (PTX) has been suggested to be a promising front-line drug for gastric cancer (GC), while P-glycoprotein (P-gp) could lead to drug resistance by pumping PTX out of GC cells. Consequently, it might be a hopeful way to combat drug resistance by inhibiting the out-pumping function of P-gp.
Results
In this study, we developed a drug delivery system incorporating PTX onto polyethylene glycol (PEG)-modified and oxidized sodium alginate (OSA) -functionalized graphene oxide (GO) nanosheets (NSs), called [email protected] Owing to pH/thermal-sensitive drug release properties, [email protected] could induced more obvious antitumor effects on GC, compared to free PTX. With near infrared (NIR)-irradiation, [email protected] could generate excessive reactive oxygen species (ROS), attack mitochondrial respiratory chain complex enzyme, reduce adenosine-triphosphate (ATP) supplement for P-gp, and effectively inhibit P-gp’s efflux pump function. Since that, [email protected] achieved better therapeutic effect on PTX-resistant GC without evident toxicity (Scheme 1).
Conclusions
In conclusion, [email protected] could serve as a desirable strategy to reverse PTX’s resistance, combined with chemo/photothermal/photodynamic therapy.

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This is a list of supplementary files associated with this preprint. Click to download.
The mechanism of [email protected] NSs during the treatment of PTX-resistant GC cells.
Schematic for the preparation of [email protected] NSs
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Posted 22 Feb, 2021
On 01 Dec, 2021
On 01 Dec, 2021
On 03 Apr, 2021
Received 18 Mar, 2021
On 06 Mar, 2021
Received 04 Mar, 2021
Received 21 Feb, 2021
Invitations sent on 21 Feb, 2021
On 20 Feb, 2021
On 11 Feb, 2021
On 07 Feb, 2021
Posted 22 Feb, 2021
On 01 Dec, 2021
On 01 Dec, 2021
On 03 Apr, 2021
Received 18 Mar, 2021
On 06 Mar, 2021
Received 04 Mar, 2021
Received 21 Feb, 2021
Invitations sent on 21 Feb, 2021
On 20 Feb, 2021
On 11 Feb, 2021
On 07 Feb, 2021
Background
Paclitaxel (PTX) has been suggested to be a promising front-line drug for gastric cancer (GC), while P-glycoprotein (P-gp) could lead to drug resistance by pumping PTX out of GC cells. Consequently, it might be a hopeful way to combat drug resistance by inhibiting the out-pumping function of P-gp.
Results
In this study, we developed a drug delivery system incorporating PTX onto polyethylene glycol (PEG)-modified and oxidized sodium alginate (OSA) -functionalized graphene oxide (GO) nanosheets (NSs), called [email protected] Owing to pH/thermal-sensitive drug release properties, [email protected] could induced more obvious antitumor effects on GC, compared to free PTX. With near infrared (NIR)-irradiation, [email protected] could generate excessive reactive oxygen species (ROS), attack mitochondrial respiratory chain complex enzyme, reduce adenosine-triphosphate (ATP) supplement for P-gp, and effectively inhibit P-gp’s efflux pump function. Since that, [email protected] achieved better therapeutic effect on PTX-resistant GC without evident toxicity (Scheme 1).
Conclusions
In conclusion, [email protected] could serve as a desirable strategy to reverse PTX’s resistance, combined with chemo/photothermal/photodynamic therapy.

Figure 1

Figure 2

Figure 3

Figure 4

Figure 5

Figure 6

Figure 7

Figure 8
This is a list of supplementary files associated with this preprint. Click to download.
The mechanism of [email protected] NSs during the treatment of PTX-resistant GC cells.
Schematic for the preparation of [email protected] NSs
Loading...