Page last updated: 2024-10-21

pd 173074 and Pancreatic Neoplasms

pd 173074 has been researched along with Pancreatic Neoplasms in 2 studies

Pancreatic Neoplasms: Tumors or cancer of the PANCREAS. Depending on the types of ISLET CELLS present in the tumors, various hormones can be secreted: GLUCAGON from PANCREATIC ALPHA CELLS; INSULIN from PANCREATIC BETA CELLS; and SOMATOSTATIN from the SOMATOSTATIN-SECRETING CELLS. Most are malignant except the insulin-producing tumors (INSULINOMA).

Research Excerpts

ExcerptRelevanceReference
" Against the background of increasing acquired resistance to FGFR1 inhibitors and our previous work, which partially demonstrated the caspase-3/PARP-mediated antitumor and antimetastatic efficacy of PD173074, a selective FGFR1 inhibitor, against ALDH-high/FGFR1-rich pancreatic ductal adenocarcinoma (PDAC) cells, we investigated the probable synthetic lethality and therapeutic efficacy of targeted PARP inhibition combined with FGFR1 blockade in patients with PDAC."1.56Targeted PARP Inhibition Combined with FGFR1 Blockade is Synthetically Lethal to Malignant Cells in Patients with Pancreatic Cancer. ( Bamodu, OA; Chao, TY; Chen, JH; Lai, SW; Lee, WH; Wu, AT; Yeh, CT, 2020)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's1 (50.00)2.80

Authors

AuthorsStudies
Lai, SW1
Bamodu, OA1
Chen, JH1
Wu, AT1
Lee, WH1
Chao, TY1
Yeh, CT1
Büchler, P1
Reber, HA1
Roth, MM1
Shiroishi, M1
Friess, H1
Hines, OJ1

Other Studies

2 other studies available for pd 173074 and Pancreatic Neoplasms

ArticleYear
Targeted PARP Inhibition Combined with FGFR1 Blockade is Synthetically Lethal to Malignant Cells in Patients with Pancreatic Cancer.
    Cells, 2020, 04-08, Volume: 9, Issue:4

    Topics: Animals; Cell Line, Tumor; Female; Humans; Mice; Pancreatic Neoplasms; Phthalazines; Piperazines; Po

2020
Target therapy using a small molecule inhibitor against angiogenic receptors in pancreatic cancer.
    Neoplasia (New York, N.Y.), 2007, Volume: 9, Issue:2

    Topics: Angiogenesis Inhibitors; Animals; Antineoplastic Agents; Apoptosis; Carcinoma; Cell Cycle; Cell Divi

2007