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Table 1 CAF-secreted soluble factors involved in resistance to targeted therapies

From: The importance of being CAFs (in cancer resistance to targeted therapies)

CAF-secreted soluble factors

Mechanism of resistance to targeted therapies

Clinical application of inhibitors: representative agents in phase2/3 clinical trials

Hepatocyte Growth Factor (HGF)

Activation of MET anti-apoptotic and pro-mitogenic downstream pathways in tumor cells

Induction of stabilization/upregulation of multiple EGFR binding partners such as Axl, EphA2, CDCP1, JAK1 and integrin Beta-4

MET (HGFR) TKIs:

Foretinib (GSK1363089)

Crizotinib (PF-02341066)

Cabozantinib (BMS-907351)

Capmatinib (INC280)

Tepotinib (EMD 1214063)

HGF targeting mAbs:

Rilotumumab (AMG 102)

Ficlatuzumab (AV-299)

L2G7 (TAK-701)

Fibroblast Growth Factors (FGFs)

Activation of FGF Receptors (mainly FGFR2) and their anti-apoptotic and pro-mitogenic downstream pathways in tumor cells

Pan-FGFR TKIs:

Erdafitinib (JNJ-42756493)

Derazantinib (ARQ087)

Rogoratinib (BAY1163877)

Dovitinib (TKI258)

AZD4547

Futibatinib (TAS-120)

Zoligratinib (Debio-1347)

Infigratinib (BGJ398)

Transforming Growth Factorβ (TGFβ)

Upregulation of lncRNAs, including the lncRNA HOTAIR, able to activate estrogen receptor function in the absence of estrogens

TGFβ Receptor inhibitors:

Galunisertib (LY2157299)

TGFβ Receptor mAbs:

Fresolimumab (GC1008)

TGFβ antisense oligonucleotides:

Trabedersen (AP 12009)

Neuregulin-1b (NRG-1b)

Increased expression of FOXA1 and HER3 in cancer cells; HER3 activation.

No inhibitors in phase 2/3 trials

Insulin Growth Factor 2 (IGF2)

Activation of IGF1R anti-apoptotic and pro-mitogenic downstream pathways in tumor cells

IGF-1R TKIs:

Linsitinib (OSI-906)

Ceritinib (LDK378)

Brigatinib (AP26113)

Platelet-Derived Growth Factor C (PDGF-C)

Activation of PDGFR and promotion of angiogenesis

PDGFR-α inhibitors:

Imatinib (STI571)

Ponatinib (AP24534)

Nintedanib (BIBF 1120)

Crenolanib (CP-868596)

Masitinib (AB1010)

IL-6 family members

Expansion of the stem cell pool via JAK1/STAT3 signaling

Activation of NF-kB and AKT pathways in cancer cells

IL-6 targeting mAb:

Siltuximab (CNTO 328)

JAK1/2 inhibitors:

Ruxolitinib (INC424, INCB1842)

Chemokine (C-X-C motif) ligand 13 (CXCL13)

Recruitment of B lymphocytes that produce pro-survival cytokines

No inhibitors in phase 2/3 trials

Secreted Frizzled Related Protein 2 (sFRP2)

Wnt Antagonist, Loss Of The Key Redox Effector APE1 And Attenuated Response To ROS-Induced DNA Damage

No inhibitors in phase 2/3 trials