Table 2.
Therapeutic target | Therapeutic agent | Investigation status | Underlying mechanism | Treatment | Result of treatment | Ref. |
ATOH1 | Lentiviral vector-based | Preclinical investigation | Overexpression of ATOH1 mediates its transcriptional activity to downstream genes and induces the differentiation of GATICs | Lentiviral vector-based overexpression of ATOH1 | (1) Induction of CD44+/Lgr5+ GATICs differentiation (2) Reduced tumorigenicity of GATICs both in vitro and in vivo | Han et al[115] |
PGK1 | Lentiviral vector-based | Preclinical investigation | Knockdown of PGK1 alters the glycolytic metabolism of GATICs not only induces GATIC differentiation but also improve their chemosensitivity | Lentiviral vector-based knockdown of PGK1 | (1) Induction of CD44+ GATICs differentiation (2) Inhibited tumor growth and metastasis in vivo | Zieker et al[116] |
CD44v | Sulfasalazine | Phase I dose-escalation clinical study in EPOC1205 | Targeting CD44v by inhibiting xCT which mainly interacts with CD44v and maintains high level of GSH | 12 g/d, 4x/d with 2 wk as one cycle, oral administration | Reduced level of CD44v positive GATICs in some patients | Shitara et al[130] |
EpCam | Catumaxomab | Phase II/III clinical trial of advanced gastric carcinoma_NCT00836654 | Direct targeting CD3 and EpCam | Paracentesis +/- Catumaxomab | Clinical benefit (prolonged PFS and less symptoms of ascites) in GC patients with secondary malignant ascites | Heiss et al[131] |
EpCam | Catumaxomab | Phase II clinical trial of advanced gastric carcinoma_NCT01784900 | Direct targeting CD3 and EpCam | Surgical resection followed by Catumaxomab | Intra-/postoperative administration of catumaxomab within multimodal treatment is feasible and tolerable | Goéré et al[132] |
c-MET | Rilotumumab | Phase III clinical trial of locally advanced or metastatic gastric and GEJ carcinoma_NCT01697072 | Competitively targeting hepatocyte growth factor (HGF), ligand of c-MET receptor | ECX +/- Rilotumumab | Stopped early due to increased death risk | Doshi et al[133] |
c-MET | Onartuzumab | Phase III clinical trial of metastatic HER2(-) and c-MET(+) Gastroesophageal Cancer_NCT01662869 | Direct targeting c-MET as a MET antagonist | FOLFOX6 +/- Rilotumumab | Insignificant prolong of PFS (6.9 mo vs 5.7 mo) and OS (11.0 mo vs 9.7 mo) | Shah et al[134] |
c-MET | Tivantinib | Phase I/II clinical trial of advanced and metastatic adenocarcinoma of distal esophagus, GEJ and stomach_NCT01611857 | Inhibition of c-Met receptor tyrosine kinase | FOLFOX6 combined with Tivantinib | PFS: 6.1 mo and OS: 9.6 mo | Pant et al[135] |
SHH signaling pathway | Cyclopamine | Preclinical investigation | Targeting overexpressed Ptch/Gli1 (key effectors in SHH pathway) | Direct addition of cyclopamine (5 μmol/L in vitro and 10 μmol/L in vivo) | (1) Reduced self-renewing capacity of GATIC-enriched tumor sphere (2) Enhanced efficacy of Oxaliplatin/Mitomycin inhibiting proliferation of tumor sphere | Song et al[80] |
SHH signaling pathway | Vismodegib | Phase II clinical trial of advanced gastric and GEJ carcinoma_NCT00982592 | Targeting Smoothened (SMO) and its downstream GLI family members | FOLFOX +/- Vismodegib | (1) No significant improvement of anti-tumor activity (2) Potentially reverse the chemotherapy resistance of patients with high CD44-expressing tumor cells | Cohen et al[136] |
Wnt/β-catenin signaling pathway | Salinomycin | Preclinical investigation | Blocking and degrading LRP6 (Wnt co-receptor) | Direct addition of Salinomycin (ranging from 1 μmol/L to 100 μmol/L in vitro) | Effectively kill ALDH-high GATICs which are resistant to 5-FU and CDDP | Mao et al[87] |
Wnt/β-catenin signaling pathway | ICG-001 | Preclinical investigation | Inhibiting CBP (co-activator of Wnt/β-catenin pathway) | Direct addition of ICG-001 (50 mg/kg/d, in vivo) | (1) Suppressed GC cell growth and metastasis both in vitro and in vivo (2) Reduced self-renewal capacity and enhanced efficacy of 5-Fu/cisplatin | Liu et al[122] |
STAT3 signaling pathway | Napabucasin | Phase Ib/II dose-escalation and extension study of advanced gastric and GEJ carcinoma_NCT01325441 | Direct targeting Stat3, β-catenin and NANOG | Paclitaxel +/- Napabucasin | (1) Well-tolerated by GC patients even receiving high doses of chemotherapy (2) Observed anti-tumor activity but still needs to be further confirmed in the on-going BRIGHTER phase III clinical trial | Shah et al[137] |
GATIC: Gastric tumor-initiating cell; SHH: Sonic hedgehog; GEJ: Gastroesophageal junction; GC: Gastric cancer; ALDH: Aldehyde dehydrogenase.