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©The Author(s) 2026.
World J Gastrointest Oncol. Feb 15, 2026; 18(2): 115944
Published online Feb 15, 2026. doi: 10.4251/wjgo.v18.i2.115944
Published online Feb 15, 2026. doi: 10.4251/wjgo.v18.i2.115944
Table 1 Summary of preclinical and clinical studies investigating the antitumor and immunomodulatory effects of propofol in gastric cancer
| Ref. | Key findings | Method |
| Ni et al[11] | Suppresses cell invasion via MMP-2 inhibition through miR-29 | In vitro |
| Liu et al[12] | Inhibits tumor growth via the circPDSS1/miR-1324/SOX4 axis | In vitro |
| Xian et al[15] | Reduces proliferation through YAP1 inhibition mediated by miR-205 | In vitro |
| Zhan et al[16] | Inhibits tumor progression through the miR-493-3p/DKK1/Wnt-β-catenin axis | In vitro |
| Zhang et al[17] | Increases cisplatin sensitivity via lncRNA MALAT1/miR-30e/ATG5 pathway | In vitro + chemotherapy sensitivity |
| Ai et al[19] | Enhances antitumor immunity by increasing NK cell activity | Clinical study |
| Zheng et al[18] | Propofol-TIVA associated with better postoperative outcomes | Retrospective clinical |
| Liu and Yang[29] | Provides more stable glucose and cytokine profiles (in diabetic patients) | Clinical study |
| Li et al[27] | Observed improved neurocognitive recovery | Clinical study |
| Cao et al[14] | Suppresses tumor proliferation via NRF2 | In vitro |
Table 2 Overview of experimental and clinical studies assessing the effects of sevoflurane on gastric cancer biology and immune responses
| Ref. | Key findings | Method |
| Chen et al[20] | Increased miR-34a → Suppression of TGIF2 → Reduced EMT and invasion | In vitro |
| Liu and Chen[21] | Tumor suppression via DLX6-AS1/epigenetic modulation through ZC3H13 knockdown | In vitro |
| Yong et al[23] | Decreased FOXP3 expression in tumor cells leads to reduced invasion | In vitro |
| Yong et al[22] | Increased CD4+CD25+FOXP3+ Treg cells; indicates immune modulation | Clinical study |
Table 3 Comparative clinical studies evaluating perioperative and oncologic outcomes of propofol vs sevoflurane in gastric cancer surgery
| Ref. | Key findings | Method |
| Wang et al[10] | No difference in long-term survival; propofol group had more PONV | Retrospective clinical |
| Zheng et al[18] | Fewer inflammatory complications and better postoperative recovery with propofol | Retrospective clinical |
| Wu et al[25] | Propofol group showed better long-term survival | Retrospective clinical |
| Oh et al[26] | One-year mortality lower with propofol | Retrospective analysis |
| Ai and Wang[19] | Propofol → Higher NK cell activity (immune advantage) | Prospective clinical |
| Song et al[28] | No significant difference in AKI incidence | Retrospective matched analysis |
| Li et al[27] | Propofol → Better cognitive and emotional postoperative recovery | Clinical study |
- Citation: Arun O, Arun F. Does anesthesia choice shape oncologic destiny in gastric cancer surgery? World J Gastrointest Oncol 2026; 18(2): 115944
- URL: https://www.wjgnet.com/1948-5204/full/v18/i2/115944.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v18.i2.115944
