Temsirolimus (BioDeep_00000010491)

 

Secondary id: BioDeep_00000858820

human metabolite blood metabolite Chemicals and Drugs


代谢物信息卡片


(1R,2R,4S)-4-[(2R)-2-[(1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18-dihydroxy-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-2,3,10,14,20-pentaoxo-11,36-dioxa-4-azatricyclo[30.3.1.0⁴,⁹]hexatriaconta-16,24,26,28-tetraen-12-yl]propyl]-2-methoxycyclohexyl 3-hydroxy-2-(hydroxymethyl)-2-methylpropanoate

化学式: C56H87NO16 (1029.6025)
中文名称: 替西罗莫司
谱图信息: 最多检出来源 Homo sapiens(blood) 100%

分子结构信息

SMILES: CC1CCC2CC(C(=CC=CC=CC(CC(C(=O)C(C(C(=CC(C(=O)CC(OC(=O)C3CCCCN3C(=O)C(=O)C1(O2)O)C(C)CC4CCC(C(C4)OC)OC(=O)C(C)(CO)CO)C)C)O)OC)C)C)C)OC
InChI: InChI=1S/C56H87NO16/c1-33-17-13-12-14-18-34(2)45(68-9)29-41-22-20-39(7)56(67,73-41)51(63)52(64)57-24-16-15-19-42(57)53(65)71-46(30-43(60)35(3)26-38(6)49(62)50(70-11)48(61)37(5)25-33)36(4)27-40-21-23-44(47(28-40)69-10)72-54(66)55(8,31-58)32-59/h12-14,17-18,26,33,35-37,39-42,44-47,49-50,58-59,62,67H,15-16,19-25,27-32H2,1-11H3/b14-12+,17-13+,34-18+,38-26+/t33-,35-,36-,37-,39-,40+,41+,42+,44-,45+,46+,47-,49-,50+,56-/m1/s1

描述信息

Temsirolimus is an intravenous drug for the treatment of renal cell carcinoma (RCC), developed by Wyeth Pharmaceuticals and approved by the FDA in late May 2007, and was also approved by the European Medicines Agency (EMEA) on November 2007. It is a derivative of sirolimus and is sold as Torisel.
L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01E - Protein kinase inhibitors > L01EG - Mammalian target of rapamycin (mtor) kinase inhibitors
C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor > C61074 - Serine/Threonine Kinase Inhibitor
C274 - Antineoplastic Agent > C163758 - Targeted Therapy Agent > C2201 - mTOR Inhibitor
D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents
D004791 - Enzyme Inhibitors > D047428 - Protein Kinase Inhibitors
D000970 - Antineoplastic Agents > D000091203 - MTOR Inhibitors
Same as: D06068
Temsirolimus is an inhibitor of mTOR with an IC50 of 1.76 μM. Temsirolimus activates autophagy and prevents deterioration of cardiac function in animal model[8].
Temsirolimus is an inhibitor of mTOR with an IC50 of 1.76 μM. Temsirolimus activates autophagy and prevents deterioration of cardiac function in animal model[8].

同义名列表

10 个代谢物同义名

(1R,2R,4S)-4-[(2R)-2-[(1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18-dihydroxy-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-2,3,10,14,20-pentaoxo-11,36-dioxa-4-azatricyclo[30.3.1.0⁴,⁹]hexatriaconta-16,24,26,28-tetraen-12-yl]propyl]-2-methoxycyclohexyl 3-hydroxy-2-(hydroxymethyl)-2-methylpropanoate; 42-[3-Hydroxy-2-(hydroxymethyl)-2-methylpropanoic acid]rapamycin; Rapamycin, 42-(3-hydroxy-2-(hydroxymethyl)-2-methylpropanoate); 42-[3-Hydroxy-2-(hydroxymethyl)-2-methylpropanoate]rapamycin; Wyeth brand OF temsirolimus; Temsirolimus; CCI-779; Torisel; CCI 779; Temsirolimus



数据库引用编号

19 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

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PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

1 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 17 AKT1, ANG, CCND1, CYP3A4, EGFR, EIF4EBP1, ERBB2, PIK3C3, PIK3CA, PIK3R6, PTEN, RPS6KB1, TNK1, TP53, TSC1, TSC2, VEGFA
Peripheral membrane protein 4 PIK3R6, TNK1, TSC1, TSC2
Endosome membrane 2 EGFR, ERBB2
Endoplasmic reticulum membrane 2 CYP3A4, EGFR
Cytoplasmic vesicle, autophagosome 1 PIK3C3
Nucleus 12 AKT1, ANG, CCND1, EGFR, EIF4EBP1, ERBB2, PTEN, RPS6KB1, TP53, TSC1, TSC2, VEGFA
autophagosome 1 PIK3C3
cytosol 13 AKT1, ANG, CCND1, EIF4EBP1, ERBB2, PIK3C3, PIK3CA, PIK3R6, PTEN, RPS6KB1, TP53, TSC1, TSC2
phosphatidylinositol 3-kinase complex, class III 1 PIK3C3
centrosome 2 CCND1, TP53
nucleoplasm 6 AKT1, CCND1, ERBB2, PTEN, RPS6KB1, TP53
Cell membrane 4 AKT1, EGFR, ERBB2, PIK3R6
lamellipodium 3 AKT1, PIK3CA, TSC1
ruffle membrane 2 EGFR, ERBB2
Early endosome membrane 1 EGFR
cell cortex 2 AKT1, TSC1
cell junction 1 EGFR
cell surface 3 EGFR, RPS6KB1, VEGFA
glutamatergic synapse 4 AKT1, EGFR, PIK3C3, RPS6KB1
Golgi apparatus 2 TSC2, VEGFA
Golgi membrane 1 EGFR
growth cone 1 ANG
lysosomal membrane 2 TSC1, TSC2
neuromuscular junction 1 ERBB2
neuronal cell body 1 ANG
postsynapse 2 AKT1, RPS6KB1
presynaptic membrane 1 ERBB2
Cytoplasm, cytosol 2 TSC1, TSC2
Lysosome 1 TSC2
endosome 2 EGFR, PIK3C3
plasma membrane 9 AKT1, EGFR, ERBB2, IFNLR1, PIK3CA, PIK3R6, PTEN, TNK1, TSC1
Membrane 12 AKT1, CYP3A4, EGFR, ERBB2, IFNLR1, PIK3C3, PIK3R6, TNK1, TP53, TSC1, TSC2, VEGFA
apical plasma membrane 3 EGFR, ERBB2, PTEN
basolateral plasma membrane 2 EGFR, ERBB2
Lysosome membrane 2 TSC1, TSC2
endoplasmic reticulum 2 TP53, VEGFA
extracellular space 5 ANG, EGFR, IFNA1, IL2, VEGFA
perinuclear region of cytoplasm 6 EGFR, ERBB2, PIK3CA, RPS6KB1, TSC1, TSC2
adherens junction 1 VEGFA
bicellular tight junction 1 CCND1
intercalated disc 1 PIK3CA
mitochondrion 2 RPS6KB1, TP53
protein-containing complex 4 AKT1, EGFR, TP53, TSC1
intracellular membrane-bounded organelle 1 CYP3A4
Microsome membrane 1 CYP3A4
postsynaptic density 3 PTEN, TSC1, TSC2
Single-pass type I membrane protein 3 EGFR, ERBB2, IFNLR1
Secreted 4 ANG, IFNA1, IL2, VEGFA
extracellular region 5 ANG, ERBB2, IL2, PTEN, VEGFA
cytoplasmic side of plasma membrane 1 PTEN
mitochondrial outer membrane 1 RPS6KB1
Mitochondrion matrix 1 TP53
mitochondrial matrix 1 TP53
transcription regulator complex 1 TP53
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 1 TP53
Nucleus membrane 1 CCND1
nuclear membrane 2 CCND1, EGFR
Secreted, extracellular space, extracellular matrix 1 VEGFA
actin cytoskeleton 1 ANG
dendritic spine 1 PTEN
cytoplasmic vesicle 1 ERBB2
microtubule cytoskeleton 1 AKT1
nucleolus 2 ANG, TP53
midbody 1 PIK3C3
Early endosome 1 ERBB2
cell-cell junction 1 AKT1
vesicle 1 AKT1
Cell projection, ruffle membrane 1 ERBB2
Cytoplasm, perinuclear region 1 ERBB2
Membrane raft 1 EGFR
Cytoplasm, cytoskeleton 1 TP53
focal adhesion 1 EGFR
spindle 1 AKT1
GABA-ergic synapse 1 PIK3C3
extracellular matrix 1 VEGFA
Peroxisome 1 PIK3C3
basement membrane 1 ANG
intracellular vesicle 1 EGFR
Cell projection, dendritic spine 1 PTEN
Nucleus, PML body 2 PTEN, TP53
PML body 2 PTEN, TP53
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 1 AKT1
secretory granule 1 VEGFA
axoneme 1 PIK3C3
Late endosome 1 PIK3C3
receptor complex 2 EGFR, ERBB2
Cell projection, neuron projection 1 PTEN
neuron projection 2 PTEN, RPS6KB1
ciliary basal body 1 AKT1
chromatin 1 TP53
cell projection 1 PTEN
phagocytic vesicle membrane 1 PIK3C3
Chromosome 1 ANG
Nucleus, nucleolus 1 ANG
site of double-strand break 1 TP53
Lipid droplet 1 TSC1
phagophore assembly site 1 PIK3C3
phosphatidylinositol 3-kinase complex, class III, type I 1 PIK3C3
phosphatidylinositol 3-kinase complex, class III, type II 1 PIK3C3
Cytoplasm, Stress granule 1 ANG
cytoplasmic stress granule 1 ANG
germ cell nucleus 1 TP53
replication fork 1 TP53
myelin sheath 1 ERBB2
basal plasma membrane 2 EGFR, ERBB2
synaptic membrane 1 EGFR
nuclear matrix 1 TP53
transcription repressor complex 2 CCND1, TP53
platelet alpha granule lumen 1 VEGFA
phosphatidylinositol 3-kinase complex 2 PIK3CA, PIK3R6
phosphatidylinositol 3-kinase complex, class IA 2 PIK3CA, PIK3R6
endocytic vesicle 1 ANG
Schmidt-Lanterman incisure 1 PTEN
presynaptic endosome 1 PIK3C3
semaphorin receptor complex 1 ERBB2
clathrin-coated endocytic vesicle membrane 1 EGFR
[Isoform 1]: Nucleus 1 TP53
Synapse, synaptosome 1 RPS6KB1
protein folding chaperone complex 1 TSC1
[Isoform 1]: Cell membrane 1 ERBB2
cyclin-dependent protein kinase holoenzyme complex 1 CCND1
postsynaptic endosome 1 PIK3C3
multivesicular body, internal vesicle lumen 1 EGFR
Shc-EGFR complex 1 EGFR
Autolysosome 1 PIK3C3
angiogenin-PRI complex 1 ANG
ERBB3:ERBB2 complex 1 ERBB2
myelin sheath adaxonal region 1 PTEN
cyclin D1-CDK4 complex 1 CCND1
[Isoform alpha]: Secreted 1 PTEN
[N-VEGF]: Cytoplasm 1 VEGFA
[VEGFA]: Secreted 1 VEGFA
[Isoform L-VEGF189]: Endoplasmic reticulum 1 VEGFA
[Isoform VEGF121]: Secreted 1 VEGFA
[Isoform VEGF165]: Secreted 1 VEGFA
VEGF-A complex 1 VEGFA
cyclin D1-CDK6 complex 1 CCND1
phosphatidylinositol 3-kinase complex, class IB 2 PIK3CA, PIK3R6
TSC1-TSC2 complex 2 TSC1, TSC2
interleukin-28 receptor complex 1 IFNLR1


文献列表

  • Arne Strauss, Marianne Schmid, Michael Rink, Michael Moran, Stephan Bernhardt, Marcus Hubbe, Lothar Bergmann, Katrin Schlack, Martin Boegemann. Real-world outcomes in patients with metastatic renal cell carcinoma according to risk factors: the STAR-TOR registry. Future oncology (London, England). 2021 Jun; 17(18):2325-2338. doi: 10.2217/fon-2020-1020. [PMID: 33724867]
  • Hiromasa Sakamoto, Toshinari Yamasaki, Takayuki Sumiyoshi, Masashi Takeda, Noboru Shibasaki, Noriaki Utsunomiya, Ryuichiro Arakaki, Shusuke Akamatsu, Takashi Kobayashi, Takahiro Inoue, Tomomi Kamba, Eijiro Nakamura, Osamu Ogawa. Functional and genomic characterization of patient-derived xenograft model to study the adaptation to mTORC1 inhibitor in clear cell renal cell carcinoma. Cancer medicine. 2021 01; 10(1):119-134. doi: 10.1002/cam4.3578. [PMID: 33107222]
  • Annemarie Uhlig, Johannes Uhlig, Lutz Trojan, Michael Woike, Marianne Leitsmann, Arne Strauß. Toxicities of axitinib, sunitinib and temsirolimus: implications for progression-free and overall survival in metastatic renal cell cancer. Future oncology (London, England). 2021 Jan; 17(1):45-56. doi: 10.2217/fon-2020-0900. [PMID: 33275038]
  • Fabian Hofmann, Eu Chang Hwang, Thomas Bl Lam, Axel Bex, Yuhong Yuan, Lorenzo So Marconi, Börje Ljungberg. Targeted therapy for metastatic renal cell carcinoma. The Cochrane database of systematic reviews. 2020 10; 10(?):CD012796. doi: 10.1002/14651858.cd012796.pub2. [PMID: 33058158]
  • Nizar M Tannir, Pavlos Msaouel, Jeremy A Ross, Catherine E Devine, Anuradha Chandramohan, Graciela M Nogueras Gonzalez, Xuemei Wang, Jennifer Wang, Paul G Corn, Zita D Lim, Lisa Pruitt, Jose A Karam, Christopher G Wood, Amado J Zurita. Temsirolimus versus Pazopanib (TemPa) in Patients with Advanced Clear-cell Renal Cell Carcinoma and Poor-risk Features: A Randomized Phase II Trial. European urology oncology. 2020 10; 3(5):687-694. doi: 10.1016/j.euo.2019.06.004. [PMID: 31272939]
  • Sen Chen, Long Cui, Qiao Hu, Yingying Shen, Yan Jiang, Juan Zhao. Preclinical evidence that MNK/eIF4E inhibition by cercosporamide enhances the response to antiangiogenic TKI and mTOR inhibitor in renal cell carcinoma. Biochemical and biophysical research communications. 2020 09; 530(1):142-148. doi: 10.1016/j.bbrc.2020.06.133. [PMID: 32828276]
  • Shigeru Sugiyama, Kazuo Sato, Yoshiyuki Shibasaki, Yutaka Endo, Taku Uryu, Yasuharu Toyoshima, Mototsugu Oya, Naoto Miyanaga, Nagahiro Saijo, Akihiko Gemma, Hideyuki Akaza. Real-world use of temsirolimus in Japanese patients with unresectable or metastatic renal cell carcinoma: recent consideration based on the results of a post-marketing, all-case surveillance study. Japanese journal of clinical oncology. 2020 Aug; 50(8):940-947. doi: 10.1093/jjco/hyaa062. [PMID: 32458996]
  • Yuqing Li, Yanyun Shen, Zhidong Zhu, Hui Wen, Chenchen Feng. Comprehensive analysis of copy number variance and sensitivity to common targeted therapy in clear cell renal cell carcinoma: In silico analysis with in vitro validation. Cancer medicine. 2020 08; 9(16):6020-6029. doi: 10.1002/cam4.3281. [PMID: 32628820]
  • Kazuki Kuroshima, Hirofumi Yoshino, Shunsuke Okamura, Masafumi Tsuruda, Yoichi Osako, Takashi Sakaguchi, Satoshi Sugita, Shuichi Tatarano, Masayuki Nakagawa, Hideki Enokida. Potential new therapy of Rapalink-1, a new generation mammalian target of rapamycin inhibitor, against sunitinib-resistant renal cell carcinoma. Cancer science. 2020 May; 111(5):1607-1618. doi: 10.1111/cas.14395. [PMID: 32232883]
  • Yukari Kobayashi, Daisuke Yamada, Taketo Kawai, Yusuke Sato, Taro Teshima, Yuta Yamada, Masaaki Nakamura, Motofumi Suzuki, Akihiko Matsumoto, Tohru Nakagawa, Akihiro Hosoi, Koji Nagaoka, Takahiro Karasaki, Hirokazu Matsushita, Haruki Kume, Kazuhiro Kakimi. Different immunological effects of the molecular targeted agents sunitinib, everolimus and temsirolimus in patients with renal cell carcinoma. International journal of oncology. 2020 04; 56(4):999-1013. doi: 10.3892/ijo.2020.4975. [PMID: 32319571]
  • Juan M Roldan-Romero, Benoit Beuselinck, María Santos, Juan F Rodriguez-Moreno, Javier Lanillos, Bruna Calsina, Ana Gutierrez, Karin Tang, Nuria Lainez, Javier Puente, Daniel Castellano, Emilio Esteban, Miguel A Climent, Jose A Arranz, Maarten Albersen, Stephane Oudard, Gabrielle Couchy, Eduardo Caleiras, Cristina Montero-Conde, Alberto Cascón, Mercedes Robledo, Cristina Rodríguez-Antona, Jesús García-Donas. PTEN expression and mutations in TSC1, TSC2 and MTOR are associated with response to rapalogs in patients with renal cell carcinoma. International journal of cancer. 2020 03; 146(5):1435-1444. doi: 10.1002/ijc.32579. [PMID: 31335987]
  • Po-Ming Chow, Shing-Hwa Liu, Yu-Wei Chang, Kuan-Lin Kuo, Wei-Chou Lin, Kuo-How Huang. The covalent CDK7 inhibitor THZ1 enhances temsirolimus-induced cytotoxicity via autophagy suppression in human renal cell carcinoma. Cancer letters. 2020 02; 471(?):27-37. doi: 10.1016/j.canlet.2019.12.005. [PMID: 31812697]
  • Ravneet Chhabra, Meera Nanjundan. Lysophosphatidic acid reverses Temsirolimus-induced changes in lipid droplets and mitochondrial networks in renal cancer cells. PloS one. 2020; 15(6):e0233887. doi: 10.1371/journal.pone.0233887. [PMID: 32492043]
  • Lothar Bergmann, Viktor Grünwald, Luise Maute, Marc-Oliver Grimm, Steffen Weikert, Jan Schleicher, Theodor Klotz, Jochen Greiner, Anne Flörcken, Arndt Hartmann, Thomas Gauler. A Randomized Phase IIa Trial with Temsirolimus versus Sunitinib in Advanced Non-Clear Cell Renal Cell Carcinoma: An Intergroup Study of the CESAR Central European Society for Anticancer Drug Research-EWIV and the Interdisciplinary Working Group on Renal Cell Cancer (IAGN) of the German Cancer Society. Oncology research and treatment. 2020; 43(7-8):333-339. doi: 10.1159/000508450. [PMID: 32541143]
  • Zhiping Yu, Yixuan Wang, Dan Xu, Lianhua Zhu, Ming Hu, Qiuli Liu, Weihua Lan, Jun Jiang, Luofu Wang. G250 Antigen-Targeting Drug-Loaded Nanobubbles Combined with Ultrasound Targeted Nanobubble Destruction: A Potential Novel Treatment for Renal Cell Carcinoma. International journal of nanomedicine. 2020; 15(?):81-95. doi: 10.2147/ijn.s230879. [PMID: 32021166]
  • In Hee Lee, Byung Woog Kang, Jong Gwang Kim, Woo Kyun Bae, Myung Seo Ki, Inkeun Park, Jae-Cheol Jo, Jin Young Kim, Sung Ae Koh, Kyung Hee Lee, Yoon Young Cho, Hun Mo Ryoo, Sang Gyu Kwak, Jung Lim Lee, Sun Ah Lee. Comparison of three risk stratification models for non-clear cell renal cell carcinoma patients treated with temsirolimus as first-line therapy. The Korean journal of internal medicine. 2020 01; 35(1):185-193. doi: 10.3904/kjim.2018.064. [PMID: 30301310]
  • Orsolya Basa-Dénes, Réka Angi, Balázs Kárpáti, Tamás Jordán, Zsolt Ötvös, Nikoletta Erdősi, Andrea Ujhelyi, Betti Ordasi, László Molnár, John McDermott, Chris Roe, Litza McKenzie, Tamás Solymosi, Gábor Heltovics, Hristos Glavinas. Dose Escalation Study to Assess the Pharmacokinetic Parameters of a Nano-amorphous Oral Sirolimus Formulation in Healthy Volunteers. European journal of drug metabolism and pharmacokinetics. 2019 Dec; 44(6):777-785. doi: 10.1007/s13318-019-00562-y. [PMID: 31089971]
  • Sherrie L Aspinall, Xinhua Zhao, Mark C Geraci, Chester B Good, Francesca E Cunningham, Bernadette B Heron, Daniel Becker, Steve Lee, Vinay Prasad. Use of targeted therapies for advanced renal cell carcinoma in the Veterans Health Administration. Cancer medicine. 2019 11; 8(15):6651-6661. doi: 10.1002/cam4.2531. [PMID: 31536684]
  • Nikolina Basic-Jukic, Ines Mesar, Jason Kirincich. Cutaneous Metastasis as a Presenting Feature of Renal Adenocarcinoma in a Renal Transplant Recipient: A Case Report. Transplantation proceedings. 2019 Nov; 51(9):3072-3073. doi: 10.1016/j.transproceed.2019.04.021. [PMID: 31611123]
  • Jii Bum Lee, Hyung Soon Park, Sejung Park, Hyo Jin Lee, Kyung A Kwon, Young Jin Choi, Yu Jung Kim, Chung Mo Nam, Nam Hoon Cho, Beodeul Kang, Hyun Cheol Chung, Sun Young Rha. Temsirolimus in Asian Metastatic/Recurrent Non-clear Cell Renal Carcinoma. Cancer research and treatment. 2019 Oct; 51(4):1578-1588. doi: 10.4143/crt.2018.671. [PMID: 30999721]
  • Niels Fristrup, Frede Donskov. Folic Acid Reduces Mucositis in Metastatic Renal Cell Carcinoma Patients: A Retrospective Study. Clinical genitourinary cancer. 2019 08; 17(4):254-259. doi: 10.1016/j.clgc.2019.03.023. [PMID: 31101577]
  • Jiangjin Li, Xiaoli Xiang, Zuo Xu. Cilostazol protects against myocardial ischemia and reperfusion injury by activating transcription factor EB (TFEB). Biotechnology and applied biochemistry. 2019 Jul; 66(4):555-563. doi: 10.1002/bab.1754. [PMID: 30994947]
  • Inkeun Park, Young Sup Shim, Heounjeong Go, Bum Sik Hong, Jae Lyun Lee. Long-term response of metastatic hereditary leiomyomatosis and renal cell carcinoma syndrome associated renal cell carcinoma to bevacizumab plus erlotinib after temsirolimus and axitinib treatment failures. BMC urology. 2019 Jun; 19(1):51. doi: 10.1186/s12894-019-0484-2. [PMID: 31182090]
  • Julie Bastin, Emilie Werbrouck, Annelies Verbiest, Kevin Punie, Oliver Bechter, Feng Jung Woei-A-Jin, Pascal Wolter, Hans Wildiers, Evelyne Lerut, Herlinde Dumez, Brigitte Decallonne, Paul Clement, Dirk Vanderschueren, Maarten Albersen, Raymond Oyen, Patrick Schöffski, Benoit Beuselinck. Prospective evaluation of hypogonadism in male metastatic renal cell carcinoma patients treated with targeted therapies. Acta clinica Belgica. 2019 Jun; 74(3):169-179. doi: 10.1080/17843286.2018.1476115. [PMID: 29774795]
  • Aristotelis Bamias, Vasilios Karavasilis, Nikolaos Gavalas, Kimon Tzannis, Epaminontas Samantas, Gerasimos Aravantinos, Angelos Koutras, Ioannis Gkerzelis, Euthymios Kostouros, Konstantinos Koutsoukos, Flora Zagouri, George Fountzilas, Meletios-Athanasios Dimopoulos. The combination of bevacizumab/temsirolimus after first-line anti-VEGF therapy in advanced renal-cell carcinoma: a clinical and biomarker study. International journal of clinical oncology. 2019 Apr; 24(4):411-419. doi: 10.1007/s10147-018-1361-9. [PMID: 30374686]
  • So-Yeon Jeon, Na-Ri Lee, Chang-Yeol Yim. Successful re-administration of Pazopanib in a patient with metastatic renal cell carcinoma and a history of Pazopanib-induced nephrotic syndrome: a case report. BMC nephrology. 2019 01; 20(1):1. doi: 10.1186/s12882-018-1181-1. [PMID: 30606155]
  • Lana Hamieh, Toni K Choueiri, Barbara Ogórek, Damir Khabibullin, Daniel Rosebrock, Dimitri Livitz, Andre Fay, Jean-Christophe Pignon, David F McDermott, Neeraj Agarwal, Wenhua Gao, Sabina Signoretti, David J Kwiatkowski. Mechanisms of acquired resistance to rapalogs in metastatic renal cell carcinoma. PLoS genetics. 2018 09; 14(9):e1007679. doi: 10.1371/journal.pgen.1007679. [PMID: 30256787]
  • Anas Shamsi, Azaj Ahmed, Bilqees Bano. Probing the interaction of anticancer drug temsirolimus with human serum albumin: molecular docking and spectroscopic insight. Journal of biomolecular structure & dynamics. 2018 May; 36(6):1479-1489. doi: 10.1080/07391102.2017.1326320. [PMID: 28464730]
  • Pablo Maroto, Georgia Anguera, Juan Maria Roldan-Romero, Maria Apellániz-Ruiz, Ferran Algaba, Jacqueline Boonman, Mark Nellist, Cristina Montero-Conde, Alberto Cascón, Mercedes Robledo, Cristina Rodríguez-Antona. Biallelic TSC2 Mutations in a Patient With Chromophobe Renal Cell Carcinoma Showing Extraordinary Response to Temsirolimus. Journal of the National Comprehensive Cancer Network : JNCCN. 2018 04; 16(4):352-358. doi: 10.6004/jnccn.2017.7041. [PMID: 29632054]
  • Anas Shamsi, Azaj Ahmed, Bilqees Bano. Global transition of human serum albumin to prefibrillar aggregates induced by temsirolimus: Insight into implications of anti-renal cancer drug. Journal of molecular recognition : JMR. 2018 04; 31(4):. doi: 10.1002/jmr.2688. [PMID: 29178153]
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