腫瘍随伴マクロファージ (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "腫瘍随伴マクロファージ" in Japanese language version.

refsWebsite

Global rank Japanese rank

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24^th place

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6^th place

1semanticscholar.org

11^th place

1,537^th place

1clinicaltrials.gov

5,225^th place

low place

low place

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clinicaltrials.gov (Global: 5,225^th place; Japanese: low place)

臨床試験番号 NCT03158272 研究名 "A Study to of Cabiralzumab Given by Itself or With Nivolumab in Advanced Cancer or Cancer That Has Spread" - ClinicalTrials.gov

doi.org (Global: 2^nd place; Japanese: 6^th place)

“Tumor-associated macrophages: Potential therapeutic targets for anti-cancer therapy”. Advanced Drug Delivery Reviews 99 (Pt B): 180–185. (April 2016). doi:10.1016/j.addr.2015.11.009. PMID 26621196.
“Macrophages and cancer: from mechanisms to therapeutic implications”. Trends in Immunology 36 (4): 229–39. (April 2015). doi:10.1016/j.it.2015.02.004. PMID 25770924.
“Macrophage diversity enhances tumor progression and metastasis”. Cell 141 (1): 39–51. (April 2010). doi:10.1016/j.cell.2010.03.014. PMC 4994190. PMID 20371344.
“Tumour-associated macrophages as treatment targets in oncology”. Nature Reviews. Clinical Oncology 14 (7): 399–416. (July 2017). doi:10.1038/nrclinonc.2016.217. PMC 5480600. PMID 28117416.
“Role of tumor associated macrophages in tumor angiogenesis and lymphangiogenesis”. Frontiers in Physiology 5: 75. (5 March 2014). doi:10.3389/fphys.2014.00075. PMC 3942647. PMID 24634660.
“Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis”. Nature Cell Biology 2 (10): 737–44. (October 2000). doi:10.1038/35036374. PMC 2852586. PMID 11025665.
“Myeloid WNT7b mediates the angiogenic switch and metastasis in breast cancer”. Cancer Research 74 (11): 2962–73. (June 2014). doi:10.1158/0008-5472.CAN-13-2421. PMC 4137408. PMID 24638982.
“Tie2 identifies a hematopoietic lineage of proangiogenic monocytes required for tumor vessel formation and a mesenchymal population of pericyte progenitors”. Cancer Cell 8 (3): 211–26. (September 2005). doi:10.1016/j.ccr.2005.08.002. PMID 16169466.
“Angiopoietin 2 stimulates TIE2-expressing monocytes to suppress T cell activation and to promote regulatory T cell expansion”. Journal of Immunology 186 (7): 4183–90. (April 2011). doi:10.4049/jimmunol.1002802. PMID 21368233.
“Macrophage colony-stimulating factor augments Tie2-expressing monocyte differentiation, angiogenic function, and recruitment in a mouse model of breast cancer”. PLOS ONE 9 (6): e98623. (3 June 2014). doi:10.1371/journal.pone.0098623. PMC 4043882. PMID 24892425.
“Tumor angiogenesis and lymphangiogenesis: tumor/endothelial crosstalk and cellular/microenvironmental signaling mechanisms”. Life Sciences 92 (2): 101–7. (February 2013). doi:10.1016/j.lfs.2012.10.008. PMC 3740377. PMID 23178150.
“Crosstalk between angiogenesis and lymphangiogenesis in tumor progression”. Leukemia 18 (6): 1054–8. (June 2004). doi:10.1038/sj.leu.2403355. PMID 15057248.
“A distinct and unique transcriptional program expressed by tumor-associated macrophages (defective NF-kappaB and enhanced IRF-3/STAT1 activation)”. Blood 107 (5): 2112–22. (March 2006). doi:10.1182/blood-2005-01-0428. PMID 16269622.
“High-density gene expression analysis of tumor-associated macrophages from mouse mammary tumors”. The American Journal of Pathology 174 (3): 1048–64. (March 2009). doi:10.2353/ajpath.2009.080676. PMC 2665764. PMID 19218341.
“Activated monocytes in peritumoral stroma of hepatocellular carcinoma foster immune privilege and disease progression through PD-L1”. The Journal of Experimental Medicine 206 (6): 1327–37. (June 2009). doi:10.1084/jem.20082173. PMC 2715058. PMID 19451266.
“B7-H4 expression identifies a novel suppressive macrophage population in human ovarian carcinoma”. The Journal of Experimental Medicine 203 (4): 871–81. (April 2006). doi:10.1084/jem.20050930. PMC 2118300. PMID 16606666.
“Tumor-associated macrophages: from mechanisms to therapy”. Immunity 41 (1): 49–61. (July 2014). doi:10.1016/j.immuni.2014.06.010. PMC 4137410. PMID 25035953.
“Macrophage expression of hypoxia-inducible factor-1 alpha suppresses T-cell function and promotes tumor progression”. Cancer Research 70 (19): 7465–75. (October 2010). doi:10.1158/0008-5472.CAN-10-1439. PMC 2948598. PMID 20841473.
“Siglec-15 as an immune suppressor and potential target for normalization cancer immunotherapy”. Nature Medicine 25 (4): 656–666. (April 2019). doi:10.1038/s41591-019-0374-x. PMC 7175920. PMID 30833750.
“The M1 and M2 paradigm of macrophage activation: time for reassessment”. F1000prime Reports 6: 13. (3 March 2014). doi:10.12703/P6-13. PMC 3944738. PMID 24669294.
“The inflammatory micro-environment in tumor progression: the role of tumor-associated macrophages”. Critical Reviews in Oncology/Hematology 66 (1): 1–9. (April 2008). doi:10.1016/j.critrevonc.2007.07.004. PMID 17913510.
“Tumor-associated macrophages: unwitting accomplices in breast cancer malignancy”. NPJ Breast Cancer 2 (1). (2016-01-20). doi:10.1038/npjbcancer.2015.25. PMC 4794275. PMID 26998515.
“CSF-1R inhibition alters macrophage polarization and blocks glioma progression”. Nature Medicine 19 (10): 1264–72. (October 2013). doi:10.1038/nm.3337. PMC 3840724. PMID 24056773.
“Colony-stimulating factor 1 receptor (CSF1R) inhibitors in cancer therapy”. Journal for Immunotherapy of Cancer 5 (1): 53. (July 2017). doi:10.1186/s40425-017-0257-y. PMC 5514481. PMID 28716061.
Sankhala, Kamalesh Kumar; Blay, Jean-Yves; Ganjoo, Kristen N.; Italiano, Antoine; Hassan, Andrew Bassim; Kim, Tae Min; Ravi, Vinod; Cassier, Philippe Alexandre et al. (2017). “A phase I/II dose escalation and expansion study of cabiralizumab (cabira; FPA-008), an anti-CSF1R antibody, in tenosynovial giant cell tumor (TGCT, diffuse pigmented villonodular synovitis D-PVNS)”. Journal of Clinical Oncology 35 (15_suppl): 11078. doi:10.1200/JCO.2017.35.15_suppl.11078.
“Heterogeneity of macrophage infiltration and therapeutic response in lung carcinoma revealed by 3D organ imaging”. Nature Communications 8: 14293. (February 2017). doi:10.1038/ncomms14293. PMC 5309815. PMID 28176769.
“TLR7/8-agonist-loaded nanoparticles promote the polarization of tumour-associated macrophages to enhance cancer immunotherapy”. Nature Biomedical Engineering 2 (8): 578–588. (August 2018). doi:10.1038/s41551-018-0236-8. PMID 31015631.
“Macrophages and therapeutic resistance in cancer”. Cancer Cell 27 (4): 462–72. (April 2015). doi:10.1016/j.ccell.2015.02.015. PMC 4400235. PMID 25858805.
“Class IIa HDAC inhibition reduces breast tumours and metastases through anti-tumour macrophages”. Nature 543 (7645): 428–432. (March 2017). doi:10.1038/nature21409. PMID 28273064.

nih.gov (Global: 4^th place; Japanese: 24^th place)

pubmed.ncbi.nlm.nih.gov

“Tumor-associated macrophages: Potential therapeutic targets for anti-cancer therapy”. Advanced Drug Delivery Reviews 99 (Pt B): 180–185. (April 2016). doi:10.1016/j.addr.2015.11.009. PMID 26621196.
“Macrophages and cancer: from mechanisms to therapeutic implications”. Trends in Immunology 36 (4): 229–39. (April 2015). doi:10.1016/j.it.2015.02.004. PMID 25770924.
“Macrophage diversity enhances tumor progression and metastasis”. Cell 141 (1): 39–51. (April 2010). doi:10.1016/j.cell.2010.03.014. PMC 4994190. PMID 20371344.
“Tumour-associated macrophages as treatment targets in oncology”. Nature Reviews. Clinical Oncology 14 (7): 399–416. (July 2017). doi:10.1038/nrclinonc.2016.217. PMC 5480600. PMID 28117416.
“Role of tumor associated macrophages in tumor angiogenesis and lymphangiogenesis”. Frontiers in Physiology 5: 75. (5 March 2014). doi:10.3389/fphys.2014.00075. PMC 3942647. PMID 24634660.
“Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis”. Nature Cell Biology 2 (10): 737–44. (October 2000). doi:10.1038/35036374. PMC 2852586. PMID 11025665.
“Myeloid WNT7b mediates the angiogenic switch and metastasis in breast cancer”. Cancer Research 74 (11): 2962–73. (June 2014). doi:10.1158/0008-5472.CAN-13-2421. PMC 4137408. PMID 24638982.
“Tie2 identifies a hematopoietic lineage of proangiogenic monocytes required for tumor vessel formation and a mesenchymal population of pericyte progenitors”. Cancer Cell 8 (3): 211–26. (September 2005). doi:10.1016/j.ccr.2005.08.002. PMID 16169466.
“Angiopoietin 2 stimulates TIE2-expressing monocytes to suppress T cell activation and to promote regulatory T cell expansion”. Journal of Immunology 186 (7): 4183–90. (April 2011). doi:10.4049/jimmunol.1002802. PMID 21368233.
“Macrophage colony-stimulating factor augments Tie2-expressing monocyte differentiation, angiogenic function, and recruitment in a mouse model of breast cancer”. PLOS ONE 9 (6): e98623. (3 June 2014). doi:10.1371/journal.pone.0098623. PMC 4043882. PMID 24892425.
“Tumor angiogenesis and lymphangiogenesis: tumor/endothelial crosstalk and cellular/microenvironmental signaling mechanisms”. Life Sciences 92 (2): 101–7. (February 2013). doi:10.1016/j.lfs.2012.10.008. PMC 3740377. PMID 23178150.
“Crosstalk between angiogenesis and lymphangiogenesis in tumor progression”. Leukemia 18 (6): 1054–8. (June 2004). doi:10.1038/sj.leu.2403355. PMID 15057248.
“A distinct and unique transcriptional program expressed by tumor-associated macrophages (defective NF-kappaB and enhanced IRF-3/STAT1 activation)”. Blood 107 (5): 2112–22. (March 2006). doi:10.1182/blood-2005-01-0428. PMID 16269622.
“High-density gene expression analysis of tumor-associated macrophages from mouse mammary tumors”. The American Journal of Pathology 174 (3): 1048–64. (March 2009). doi:10.2353/ajpath.2009.080676. PMC 2665764. PMID 19218341.
“Activated monocytes in peritumoral stroma of hepatocellular carcinoma foster immune privilege and disease progression through PD-L1”. The Journal of Experimental Medicine 206 (6): 1327–37. (June 2009). doi:10.1084/jem.20082173. PMC 2715058. PMID 19451266.
“B7-H4 expression identifies a novel suppressive macrophage population in human ovarian carcinoma”. The Journal of Experimental Medicine 203 (4): 871–81. (April 2006). doi:10.1084/jem.20050930. PMC 2118300. PMID 16606666.
“Tumor-associated macrophages: from mechanisms to therapy”. Immunity 41 (1): 49–61. (July 2014). doi:10.1016/j.immuni.2014.06.010. PMC 4137410. PMID 25035953.
“Macrophage expression of hypoxia-inducible factor-1 alpha suppresses T-cell function and promotes tumor progression”. Cancer Research 70 (19): 7465–75. (October 2010). doi:10.1158/0008-5472.CAN-10-1439. PMC 2948598. PMID 20841473.
“Siglec-15 as an immune suppressor and potential target for normalization cancer immunotherapy”. Nature Medicine 25 (4): 656–666. (April 2019). doi:10.1038/s41591-019-0374-x. PMC 7175920. PMID 30833750.
“The M1 and M2 paradigm of macrophage activation: time for reassessment”. F1000prime Reports 6: 13. (3 March 2014). doi:10.12703/P6-13. PMC 3944738. PMID 24669294.
“The inflammatory micro-environment in tumor progression: the role of tumor-associated macrophages”. Critical Reviews in Oncology/Hematology 66 (1): 1–9. (April 2008). doi:10.1016/j.critrevonc.2007.07.004. PMID 17913510.
“Tumor-associated macrophages: unwitting accomplices in breast cancer malignancy”. NPJ Breast Cancer 2 (1). (2016-01-20). doi:10.1038/npjbcancer.2015.25. PMC 4794275. PMID 26998515.
“CSF-1R inhibition alters macrophage polarization and blocks glioma progression”. Nature Medicine 19 (10): 1264–72. (October 2013). doi:10.1038/nm.3337. PMC 3840724. PMID 24056773.
“Colony-stimulating factor 1 receptor (CSF1R) inhibitors in cancer therapy”. Journal for Immunotherapy of Cancer 5 (1): 53. (July 2017). doi:10.1186/s40425-017-0257-y. PMC 5514481. PMID 28716061.
“Heterogeneity of macrophage infiltration and therapeutic response in lung carcinoma revealed by 3D organ imaging”. Nature Communications 8: 14293. (February 2017). doi:10.1038/ncomms14293. PMC 5309815. PMID 28176769.
“TLR7/8-agonist-loaded nanoparticles promote the polarization of tumour-associated macrophages to enhance cancer immunotherapy”. Nature Biomedical Engineering 2 (8): 578–588. (August 2018). doi:10.1038/s41551-018-0236-8. PMID 31015631.
“Macrophages and therapeutic resistance in cancer”. Cancer Cell 27 (4): 462–72. (April 2015). doi:10.1016/j.ccell.2015.02.015. PMC 4400235. PMID 25858805.
“Class IIa HDAC inhibition reduces breast tumours and metastases through anti-tumour macrophages”. Nature 543 (7645): 428–432. (March 2017). doi:10.1038/nature21409. PMID 28273064.

pmc.ncbi.nlm.nih.gov

onclive.com (Global: low place; Japanese: low place)

Inman (2017年11月12日). “Novel Combination Shows Promising Responses in Pancreatic Cancer”. OncLive. 2022年4月10日閲覧。

semanticscholar.org (Global: 11^th place; Japanese: 1,537^th place)

“A distinct and unique transcriptional program expressed by tumor-associated macrophages (defective NF-kappaB and enhanced IRF-3/STAT1 activation)”. Blood 107 (5): 2112–22. (March 2006). doi:10.1182/blood-2005-01-0428. PMID 16269622.

wikipedia.org (Global: low place; Japanese: low place)

en.wikipedia.org

臨床試験番号 NCT03158272 研究名 "A Study to of Cabiralzumab Given by Itself or With Nivolumab in Advanced Cancer or Cancer That Has Spread" - ClinicalTrials.gov