niclosamide has been researched along with Cancer of Ovary in 8 studies
Niclosamide: An antihelmintic that is active against most tapeworms. (From Martindale, The Extra Pharmacopoeia, 30th ed, p48)
niclosamide : A secondary carboxamide resulting from the formal condensation of the carboxy group of 5-chlorosalicylic acid with the amino group of 2-chloro-4-nitroaniline. It is an oral anthelmintic drug approved for use against tapeworm infections.
Excerpt | Relevance | Reference |
---|---|---|
"Cytotoxicity of niclosamide and its analogs in combination with carboplatin was demonstrated in 24 patient ascites samples." | 3.81 | Niclosamide Analogs for Treatment of Ovarian Cancer. ( Arend, RC; Buchsbaum, DJ; Chettiar, S; Gangrade, A; Hassmann, CJ; Hidalgo, B; Li, PK; Regan, N; Straughn, JM; Walters Haygood, CL, 2015) |
"Knockdown of FXR1 or IGF2BP2 in ovarian cancer cells resulted in significantly reduced cell viability, adhesion, and migration." | 1.62 | Niclosamide's potential direct targets in ovarian cancer†. ( Bheemireddy, SR; Hayashi, K; MacLean, JA; Matzuk, M; Okuda, H; Plunkett, KN; Pru, C; Sekulovski, N; Yu, Z, 2021) |
"Niclosamide is an "old" antihelminthic drug that uncouples mitochondria of intestinal parasites." | 1.43 | Preclinical evaluation of a nanoformulated antihelminthic, niclosamide, in ovarian cancer. ( Bai, MY; Chao, TK; Hu, TM; Huang, RL; Lai, HC; Lin, CK; Su, PH; Wang, YC; Weng, SJ, 2016) |
"Ovarian cancer is the most lethal gynecologic malignancy, and there is an unmet clinical need to develop new therapies." | 1.43 | A Blockade of IGF Signaling Sensitizes Human Ovarian Cancer Cells to the Anthelmintic Niclosamide-Induced Anti-Proliferative and Anticancer Activities. ( Chen, L; Deng, Y; Fan, J; Haydon, RC; He, TC; Hu, X; Liao, J; Liu, H; Luu, HH; Qi, H; Qiao, M; Wang, J; Wang, Z; Wei, Q; Yan, Z; Yu, X; Zhang, F; Zhang, J; Zou, Y, 2016) |
"Epithelial ovarian cancer (EOC) is the leading cause of gynecologic cancer mortality worldwide." | 1.43 | Niclosamide and its analogs are potent inhibitors of Wnt/β-catenin, mTOR and STAT3 signaling in ovarian cancer. ( Alvarez, RD; Arend, RC; Buchsbaum, DJ; Forero, A; Gangrade, A; Hidalgo, B; Katre, AA; Kurpad, C; Landen, CN; Li, PK; Li, Y; Londoño-Joshi, AI; Samant, RS; Straughn, JM; Yang, ES, 2016) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 7 (87.50) | 24.3611 |
2020's | 1 (12.50) | 2.80 |
Authors | Studies |
---|---|
Sekulovski, N | 1 |
MacLean, JA | 1 |
Bheemireddy, SR | 1 |
Yu, Z | 1 |
Okuda, H | 2 |
Pru, C | 1 |
Plunkett, KN | 1 |
Matzuk, M | 1 |
Hayashi, K | 2 |
Arend, RC | 3 |
Londoño-Joshi, AI | 2 |
Samant, RS | 2 |
Li, Y | 2 |
Conner, M | 1 |
Hidalgo, B | 3 |
Alvarez, RD | 2 |
Landen, CN | 2 |
Straughn, JM | 3 |
Buchsbaum, DJ | 3 |
King, ML | 1 |
Lindberg, ME | 1 |
Stodden, GR | 1 |
Ebers, SD | 1 |
Johnson, A | 1 |
Montag, A | 1 |
Lengyel, E | 1 |
MacLean Ii, JA | 1 |
Walters Haygood, CL | 1 |
Gangrade, A | 2 |
Chettiar, S | 1 |
Regan, N | 1 |
Hassmann, CJ | 1 |
Li, PK | 2 |
Lin, CK | 1 |
Bai, MY | 1 |
Hu, TM | 1 |
Wang, YC | 2 |
Chao, TK | 1 |
Weng, SJ | 1 |
Huang, RL | 2 |
Su, PH | 1 |
Lai, HC | 2 |
Deng, Y | 1 |
Wang, Z | 1 |
Zhang, F | 1 |
Qiao, M | 1 |
Yan, Z | 1 |
Wei, Q | 1 |
Wang, J | 1 |
Liu, H | 1 |
Fan, J | 1 |
Zou, Y | 1 |
Liao, J | 1 |
Hu, X | 1 |
Chen, L | 1 |
Yu, X | 1 |
Haydon, RC | 1 |
Luu, HH | 1 |
Qi, H | 1 |
He, TC | 1 |
Zhang, J | 1 |
Katre, AA | 1 |
Kurpad, C | 1 |
Yang, ES | 1 |
Forero, A | 1 |
Yo, YT | 1 |
Lin, YW | 1 |
Balch, C | 1 |
Chan, MW | 1 |
Sytwu, HK | 1 |
Chen, CK | 1 |
Chang, CC | 1 |
Nephew, KP | 1 |
Huang, T | 1 |
Yu, MH | 1 |
8 other studies available for niclosamide and Cancer of Ovary
Article | Year |
---|---|
Niclosamide's potential direct targets in ovarian cancer†.
Topics: Animals; Antineoplastic Agents; Cell Line, Tumor; Female; Humans; Mice; Niclosamide; Ovarian Neoplas | 2021 |
Inhibition of Wnt/β-catenin pathway by niclosamide: a therapeutic target for ovarian cancer.
Topics: AC133 Antigen; Aldehyde Dehydrogenase; Antigens, CD; Antineoplastic Combined Chemotherapy Protocols; | 2014 |
WNT7A/β-catenin signaling induces FGF1 and influences sensitivity to niclosamide in ovarian cancer.
Topics: Animals; beta Catenin; Cell Proliferation; Cells, Cultured; Disease Progression; Drug Resistance, Ne | 2015 |
Niclosamide Analogs for Treatment of Ovarian Cancer.
Topics: Adenocarcinoma, Clear Cell; Aged; Antinematodal Agents; Antineoplastic Agents; Ascites; beta Catenin | 2015 |
Preclinical evaluation of a nanoformulated antihelminthic, niclosamide, in ovarian cancer.
Topics: Animals; Antineoplastic Agents; Biological Availability; Cell Line, Tumor; Cell Proliferation; Drug | 2016 |
A Blockade of IGF Signaling Sensitizes Human Ovarian Cancer Cells to the Anthelmintic Niclosamide-Induced Anti-Proliferative and Anticancer Activities.
Topics: Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Antiparasitic Agents | 2016 |
Niclosamide and its analogs are potent inhibitors of Wnt/β-catenin, mTOR and STAT3 signaling in ovarian cancer.
Topics: Animals; Antineoplastic Agents; Apoptosis; beta Catenin; Cell Cycle Checkpoints; Cell Line, Tumor; C | 2016 |
Growth inhibition of ovarian tumor-initiating cells by niclosamide.
Topics: Animals; Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Cluster Analysis; Drug Screeni | 2012 |