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niacinamide and Endometrial Neoplasms

niacinamide has been researched along with Endometrial Neoplasms in 5 studies

nicotinamide : A pyridinecarboxamide that is pyridine in which the hydrogen at position 3 is replaced by a carboxamide group.

Endometrial Neoplasms: Tumors or cancer of ENDOMETRIUM, the mucous lining of the UTERUS. These neoplasms can be benign or malignant. Their classification and grading are based on the various cell types and the percent of undifferentiated cells.

Research Excerpts

ExcerptRelevanceReference
"Sorafenib is an FDA-approved multitarget tyrosine and serine/threonine kinase inhibitor currently used to treat hepatocellular carcinoma, advanced renal carcinoma and radioactive iodine-resistant thyroid carcinoma."1.46Autophagy orchestrates adaptive responses to targeted therapy in endometrial cancer. ( Bergadà, L; Boyd, J; Chen, BJ; Dolcet, X; Encinas, M; Eritja, N; Gatius, S; Llobet-Navàs, D; Martí, MD; Matias-Guiu, X; Ponce, J; Reventós, J; Ribera, J; Rodríguez-Barrueco, R; Santacana, M; Vidal, A; Villanueva, A; Yeramian, A, 2017)
"We exposed a panel of 12 endometrial cancer cell lines to a PI3K/mTOR inhibitor (voxtalisib, SAR245409) and/or a MEK inhibitor (pimasertib)."1.42Antitumor activity of a combination of dual PI3K/mTOR inhibitor SAR245409 and selective MEK1/2 inhibitor pimasertib in endometrial carcinomas. ( Arimoto, T; Fujii, T; Fukuda, T; Ikeda, Y; Inaba, K; Kashiyama, T; Kawana, K; Kuramoto, H; Miyasaka, A; Oda, K; Osuga, Y; Sone, K; Uehara, Y; Wada-Hiraike, O; Yano, T, 2015)
"Sorafenib treatment correlated with a downregulation of both FLICE-Inhibitory Protein (FLIP) and myeloid cell leukaemia-1 (Mcl-1), caused by a proteasomal degradation of both proteins."1.36The multikinase inhibitor Sorafenib induces apoptosis and sensitises endometrial cancer cells to TRAIL by different mechanisms. ( Dolcet, X; Domingo, M; Eritja, N; Gonzalez-Tallada, FJ; Llobet, D; Matias-Guiu, X; Pallares, J; Santacana, M; Sorolla, A; Yeramian, A, 2010)

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's5 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Sun, NK1
Huang, SL1
Chang, TC1
Chao, CC1
Inaba, K1
Oda, K1
Ikeda, Y1
Sone, K1
Miyasaka, A1
Kashiyama, T1
Fukuda, T1
Uehara, Y1
Arimoto, T1
Kuramoto, H1
Wada-Hiraike, O1
Kawana, K1
Yano, T1
Osuga, Y1
Fujii, T1
Mirantes, C1
Dosil, MA1
Eritja, N3
Felip, I1
Gatius, S2
Santacana, M3
Matias-Guiu, X3
Dolcet, X3
Chen, BJ1
Rodríguez-Barrueco, R1
Vidal, A1
Martí, MD1
Ponce, J1
Bergadà, L1
Yeramian, A2
Encinas, M1
Ribera, J1
Reventós, J1
Boyd, J1
Villanueva, A1
Llobet-Navàs, D1
Llobet, D1
Pallares, J1
Sorolla, A1
Domingo, M1
Gonzalez-Tallada, FJ1

Other Studies

5 other studies available for niacinamide and Endometrial Neoplasms

ArticleYear
Sorafenib induces endometrial carcinoma apoptosis by inhibiting Elk-1-dependent Mcl-1 transcription and inducing Akt/GSK3β-dependent protein degradation.
    Journal of cellular biochemistry, 2013, Volume: 114, Issue:8

    Topics: Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Endometrial Neoplasms; ets-Domain Protein Elk-1;

2013
Antitumor activity of a combination of dual PI3K/mTOR inhibitor SAR245409 and selective MEK1/2 inhibitor pimasertib in endometrial carcinomas.
    Gynecologic oncology, 2015, Volume: 138, Issue:2

    Topics: Antineoplastic Combined Chemotherapy Protocols; Cell Growth Processes; Cell Line, Tumor; Drug Synerg

2015
Effects of the multikinase inhibitors Sorafenib and Regorafenib in PTEN deficient neoplasias.
    European journal of cancer (Oxford, England : 1990), 2016, Volume: 63

    Topics: Animals; Antineoplastic Agents; Carcinoma; Cell Line, Tumor; Disease Models, Animal; Endometrial Neo

2016
Autophagy orchestrates adaptive responses to targeted therapy in endometrial cancer.
    Autophagy, 2017, Mar-04, Volume: 13, Issue:3

    Topics: Animals; Antineoplastic Agents; Autophagy; Cell Line, Tumor; Disease Progression; Endometrial Neopla

2017
The multikinase inhibitor Sorafenib induces apoptosis and sensitises endometrial cancer cells to TRAIL by different mechanisms.
    European journal of cancer (Oxford, England : 1990), 2010, Volume: 46, Issue:4

    Topics: Adenocarcinoma; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Be

2010