Genomic testing, tumor microenvironment and targeted therapy of Hedgehog-related human cancers

被引:85
作者
Katoh, Masaru [1 ]
机构
[1] Natl Canc Ctr, Dept Omics Network, Chuo Ward, 5-1-1 Tsukiji, Tokyo 1040045, Japan
关键词
ORAL SMOOTHENED INHIBITOR; BASAL-CELL CARCINOMAS; REGULATORY T-CELLS; PHASE-II TRIAL; PATHWAY INHIBITOR; SIGNALING PATHWAY; STEM-CELLS; ACQUIRED-RESISTANCE; ARSENIC TRIOXIDE; DRUG-RESISTANCE;
D O I
10.1042/CS20180845
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Hedgehog signals are transduced through Patched receptors to the Smoothened (SMO)-SUFU-GLI and SMO-Gi-RhoA signaling cascades. MTOR-S6K1 and MEK-ERK signals are also transduced to GLI activators through post-translational modifications. The GLI transcription network up-regulates target genes, such as BCL2, FOXA2, FOXE1, FOXF1, FOXL1, FOXM1, GLI1, HHIP, PTCH1 and WNT2B, in a cellular context-dependent manner. Aberrant Hedgehog signaling in tumor cells leads to self-renewal, survival, proliferation and invasion. Paracrine Hedgehog signaling in the tumor microenvironment (TME), which harbors cancer-associated fibroblasts, leads to angiogenesis, fibrosis, immune evasion and neuropathic pain. Hedgehog-related genetic alterations occur frequently in basal cell carcinoma (BCC) (85%) and Sonic Hedgehog (SHH)-subgroup medulloblastoma (87%) and less frequently in breast cancer, colorectal cancer, gastric cancer, pancreatic cancer, non-small-cell lung cancer (NSCLC) and ovarian cancer. Among investigational SMO inhibitors, vismodegib and sonidegib are approved for the treatment of patients with BCC, and glasdegib is approved for the treatment of patients with acute myeloid leukemia (AML). Resistance to SMO inhibitors is caused by acquired SMO mutations, SUFU deletions, GLI2 amplification, other by-passing mechanisms of GLI activation and WNT/beta-catenin signaling activation. GLI-DNA-interaction inhibitors (glabrescione B and GANT61), GLI2 destabilizers (arsenic trioxide and pirfenidone) and a GLI-deacetylation inhibitor (4SC-202) were shown to block GLI-dependent transcription and tumorigenesis in preclinical studies. By contrast, SMO inhibitors can remodel the immunosuppressive TME that is dominated by M2-like tumor-associated macrophages (M2-TAMs), myeloid-derived suppressor cells and regulatory T cells, and thus, a Phase I/II clinical trial of the immune checkpoint inhibitor pembrolizumab with or without vismodegib in BCC patients is ongoing.
引用
收藏
页码:953 / 970
页数:18
相关论文
共 218 条
  • [1] Loss of SUFU Function in Familial Multiple Meningioma
    Aavikko, Mervi
    Li, Song-Ping
    Saarinen, Silva
    Alhopuro, Pia
    Kaasinen, Eevi
    Morgunova, Ekaterina
    Li, Yilong
    Vesanen, Kari
    Smith, Miriam J.
    Evans, D. Gareth R.
    Poyhonen, Minna
    Kiuru, Anne
    Auvinen, Anssi
    Aaltonen, Lauri A.
    Taipale, Jussi
    Vahteristo, Pia
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2012, 91 (03) : 520 - 526
  • [2] Targeted STAT3 disruption in myeloid cells alters immunosuppressor cell abundance in a murine model of spontaneous medulloblastoma
    Abad, Catalina
    Nobuta, Hiroko
    Li, Jiaxi
    Kasai, Atsushi
    Yong, William H.
    Waschek, James A.
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 2014, 95 (02) : 357 - 367
  • [3] Context-dependent signal integration by the GLI code: The oncogenic load, pathways, modifiers and implications for cancer therapy
    Aberger, Fritz
    Ruiz i Altaba, Ariel
    [J]. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2014, 33 : 93 - 104
  • [4] Mode and specificity of binding of the small molecule GANT61 to GLI determines inhibition of GLI-DNA binding
    Agyeman, Akwasi
    Jha, Babal K.
    Mazumdar, Tapati
    Houghton, Janet A.
    [J]. ONCOTARGET, 2014, 5 (12) : 4492 - 4503
  • [5] Effects of Combined Treatment With Arsenic Trioxide and Itraconazole in Patients With Refractory Metastatic Basal Cell Carcinoma
    Ally, Mina S.
    Ransohoff, Katherine
    Sarin, Kavita
    Atwood, Scott X.
    Rezaee, Melika
    Bailey-Healy, Irene
    Kim, Jynho
    Beachy, Philip A.
    Chang, Anne Lynn S.
    Oro, Anthony
    Tang, Jean Y.
    Colevas, A. Dimitrios
    [J]. JAMA DERMATOLOGY, 2016, 152 (04) : 452 - 456
  • [6] Topical sonic hedgehog gene therapy accelerates wound healing in diabetes by enhancing endothelial progenitor cell-mediated microvascular remodeling
    Asai, Jun
    Takenaka, Hideya
    Kusano, Kengo F.
    Ii, Masaaki
    Luedemann, Corinne
    Curry, Cynthia
    Eaton, Elizabeth
    Iwakura, Atsushi
    Tsutsumi, Yoshiaki
    Hamada, Hiromichi
    Kishimoto, Saburo
    Thorne, Tina
    Kishore, Raj
    Losordo, Douglas W.
    [J]. CIRCULATION, 2006, 113 (20) : 2413 - 2424
  • [7] Smoothened Variants Explain the Majority of Drug Resistance in Basal Cell Carcinoma
    Atwood, Scott X.
    Sarin, Kavita Y.
    Whitson, Ramon J.
    Li, Jiang R.
    Kim, Geurim
    Rezaee, Melika
    Ally, Mina S.
    Kim, Jinah
    Yao, Catherine
    Chang, Anne Lynn S.
    Oro, Anthony E.
    Tang, Jean Y.
    [J]. CANCER CELL, 2015, 27 (03) : 342 - 353
  • [8] Evaluating Smoothened as a G-protein-coupled receptor for Hedgehog signalling
    Ayers, Katie L.
    Therond, Pascal P.
    [J]. TRENDS IN CELL BIOLOGY, 2010, 20 (05) : 287 - 298
  • [9] Sonic Hedgehog Promotes Desmoplasia in Pancreatic Cancer
    Bailey, Jennifer M.
    Swanson, Benjamin J.
    Hamada, Tomofumi
    Eggers, John P.
    Singh, Pankaj K.
    Caffery, Thomas
    Ouellette, Michel M.
    Hollingsworth, Michael A.
    [J]. CLINICAL CANCER RESEARCH, 2008, 14 (19) : 5995 - 6004
  • [10] Efficacy of Hedgehog Pathway Inhibitors in Basal Cell Carcinoma
    Basset-Seguin, Nicole
    Sharpe, Hayley J.
    de Sauvage, Frederic J.
    [J]. MOLECULAR CANCER THERAPEUTICS, 2015, 14 (03) : 633 - 641