vinblastin (BioDeep_00000015125)

   

PANOMIX_OTCML-2023


代谢物信息卡片


Vinblastine

化学式: C46H58N4O9 (810.4204)
中文名称: 长春质碱, 长春罗定
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 100%

分子结构信息

SMILES: CCC1(CC2CC(C3=C(CCN(C2)C1)C4=CC=CC=C4N3)(C5=C(C=C6C(=C5)C78CCN9C7C(C=CC9)(C(C(C8N6C)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC)O
InChI: InChI=1S/C46H58N4O9/c1-8-42(54)23-28-24-45(40(52)57-6,36-30(15-19-49(25-28)26-42)29-13-10-11-14-33(29)47-36)32-21-31-34(22-35(32)56-5)48(4)38-44(31)17-20-50-18-12-16-43(9-2,37(44)50)39(59-27(3)51)46(38,55)41(53)58-7/h10-14,16,21-22,28,37-39,47,54-55H,8-9,15,17-20,23-26H2,1-7H3

描述信息

L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01C - Plant alkaloids and other natural products > L01CA - Vinca alkaloids and analogues
D050258 - Mitosis Modulators > D050256 - Antimitotic Agents > D050257 - Tubulin Modulators
D000970 - Antineoplastic Agents > D050256 - Antimitotic Agents
D000970 - Antineoplastic Agents > D014748 - Vinca Alkaloids

同义名列表

6 个代谢物同义名

Vinblastine; Vinrosidine; vinblastin; Leurosidine; Vinblastine; Leurosidine



数据库引用编号

18 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

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)

0 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 10 ABCB1, ALB, ANG, BCL2L1, CASP3, CDKN1A, CYP3A4, TP53, TUBB4B, VEGFA
Peripheral membrane protein 1 CYP1B1
Endoplasmic reticulum membrane 4 CD4, CYP1B1, CYP3A4, HSP90B1
Mitochondrion membrane 1 BCL2L1
Nucleus 9 ALB, ANG, CASP3, CDKN1A, HSP90B1, KLK3, TP53, TUBB4B, VEGFA
cytosol 8 ALB, ANG, BCL2L1, CASP3, CDKN1A, HSP90B1, TP53, TUBB4B
nuclear body 1 CDKN1A
centrosome 3 ALB, BCL2L1, TP53
nucleoplasm 4 ATP2B1, CASP3, CDKN1A, TP53
Cell membrane 4 ABCB1, ABCC1, ATP2B1, CD4
Cytoplasmic side 1 BCL2L1
Multi-pass membrane protein 3 ABCB1, ABCC1, ATP2B1
Synapse 1 ATP2B1
cell surface 2 ABCB1, VEGFA
glutamatergic synapse 2 ATP2B1, CASP3
Golgi apparatus 2 ALB, VEGFA
growth cone 1 ANG
mitochondrial inner membrane 1 BCL2L1
neuronal cell body 2 ANG, CASP3
presynaptic membrane 1 ATP2B1
smooth endoplasmic reticulum 1 HSP90B1
Cytoplasm, cytosol 1 BCL2L1
plasma membrane 6 ABCB1, ABCC1, ATP2B1, CD4, IFNLR1, KLK3
synaptic vesicle membrane 2 ATP2B1, BCL2L1
Membrane 9 ABCB1, ABCC1, ATP2B1, CYP1B1, CYP3A4, HSP90B1, IFNLR1, TP53, VEGFA
apical plasma membrane 2 ABCB1, ABCC1
basolateral plasma membrane 2 ABCC1, ATP2B1
extracellular exosome 7 ABCB1, ABCC1, ALB, ATP2B1, HSP90B1, KLK3, TUBB4B
endoplasmic reticulum 5 ALB, BCL2L1, HSP90B1, TP53, VEGFA
extracellular space 7 ALB, ANG, CSF3, IFNA1, IL2, KLK3, VEGFA
lysosomal lumen 1 CSF3
perinuclear region of cytoplasm 2 CDKN1A, HSP90B1
adherens junction 1 VEGFA
mitochondrion 3 BCL2L1, CYP1B1, TP53
protein-containing complex 5 ALB, CDKN1A, HSP90B1, KLK3, TP53
intracellular membrane-bounded organelle 3 ATP2B1, CYP1B1, CYP3A4
Microsome membrane 2 CYP1B1, CYP3A4
postsynaptic density 1 CASP3
Single-pass type I membrane protein 2 CD4, IFNLR1
Secreted 6 ALB, ANG, CSF3, IFNA1, IL2, VEGFA
extracellular region 8 ALB, ANG, CSF3, HSP90B1, IL2, KLK3, TUBB4B, VEGFA
Mitochondrion outer membrane 1 BCL2L1
Single-pass membrane protein 1 BCL2L1
mitochondrial outer membrane 1 BCL2L1
Mitochondrion matrix 2 BCL2L1, TP53
mitochondrial matrix 2 BCL2L1, TP53
anchoring junction 1 ALB
transcription regulator complex 1 TP53
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 2 BCL2L1, TP53
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 2 ATP2B1, BCL2L1
Nucleus membrane 1 BCL2L1
Bcl-2 family protein complex 1 BCL2L1
nuclear membrane 1 BCL2L1
external side of plasma membrane 1 CD4
Extracellular vesicle 1 TUBB4B
Secreted, extracellular space, extracellular matrix 1 VEGFA
actin cytoskeleton 1 ANG
microtubule cytoskeleton 1 TUBB4B
nucleolus 3 ANG, CDKN1A, TP53
midbody 1 HSP90B1
Early endosome 1 CD4
Apical cell membrane 1 ABCB1
Membrane raft 1 CD4
Cytoplasm, cytoskeleton 2 TP53, TUBB4B
focal adhesion 1 HSP90B1
microtubule 1 TUBB4B
extracellular matrix 1 VEGFA
basement membrane 1 ANG
Nucleus, PML body 1 TP53
PML body 1 TP53
collagen-containing extracellular matrix 1 HSP90B1
secretory granule 2 KLK3, VEGFA
lateral plasma membrane 2 ABCC1, ATP2B1
ciliary basal body 1 ALB
chromatin 1 TP53
cell projection 1 ATP2B1
mitotic spindle 1 TUBB4B
Chromosome 1 ANG
cytoskeleton 1 TUBB4B
centriole 1 ALB
Nucleus, nucleolus 1 ANG
spindle pole 1 ALB
blood microparticle 1 ALB
Basolateral cell membrane 1 ATP2B1
site of double-strand break 1 TP53
intercellular bridge 1 TUBB4B
Cytoplasm, cytoskeleton, flagellum axoneme 1 TUBB4B
sperm flagellum 1 TUBB4B
axonemal microtubule 1 TUBB4B
Melanosome 1 HSP90B1
Cytoplasm, Stress granule 1 ANG
cytoplasmic stress granule 1 ANG
Presynaptic cell membrane 1 ATP2B1
germ cell nucleus 1 TP53
replication fork 1 TP53
sperm plasma membrane 1 HSP90B1
basal plasma membrane 1 ABCC1
endoplasmic reticulum lumen 3 ALB, CD4, HSP90B1
nuclear matrix 1 TP53
transcription repressor complex 1 TP53
platelet alpha granule lumen 2 ALB, VEGFA
endocytic vesicle 1 ANG
azurophil granule lumen 1 TUBB4B
immunological synapse 1 ATP2B1
clathrin-coated endocytic vesicle membrane 1 CD4
Sarcoplasmic reticulum lumen 1 HSP90B1
[Isoform 1]: Nucleus 1 TP53
external side of apical plasma membrane 1 ABCB1
death-inducing signaling complex 1 CASP3
cyclin-dependent protein kinase holoenzyme complex 1 CDKN1A
endocytic vesicle lumen 2 CSF3, HSP90B1
T cell receptor complex 1 CD4
angiogenin-PRI complex 1 ANG
endoplasmic reticulum chaperone complex 1 HSP90B1
photoreceptor ribbon synapse 1 ATP2B1
PCNA-p21 complex 1 CDKN1A
[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
ciliary transition fiber 1 ALB
[Isoform Bcl-X(L)]: Mitochondrion inner membrane 1 BCL2L1
interleukin-28 receptor complex 1 IFNLR1


文献列表

  • Masoomeh Nabaei, Rayhaneh Amooaghaie, Mansour Ghorbanpour, Alimohammad Ahadi. Crosstalk between melatonin and nitric oxide restrains Cadmium-induced oxidative stress and enhances vinblastine biosynthesis in Catharanthus roseus (L) G Don. Plant cell reports. 2024 May; 43(6):139. doi: 10.1007/s00299-024-03229-4. [PMID: 38735908]
  • Pooja Singh, Seema Yadav, Saumya Shah, Karuna Shanker, Velusamy Sundaresan, Ashutosh K Shukla. Characterization of a CrPME indicates its possible role in determining vindoline accumulation in Catharanthus roseus leaves. Physiologia plantarum. 2024 Mar; 176(2):e14276. doi: 10.1111/ppl.14276. [PMID: 38566244]
  • Jun Guo, Di Gao, Jiazhang Lian, Yang Qu. De novo biosynthesis of antiarrhythmic alkaloid ajmaline. Nature communications. 2024 Jan; 15(1):457. doi: 10.1038/s41467-024-44797-z. [PMID: 38212296]
  • Jawad Ahmed, Yasar Sajjad, Aasia Latif, Mohammad Saeed Lodhi, Muhammad Huzafa, Chen Situ, Raza Ahmad, Muhammad Maroof Shah, Amjad Hassan. Genome-wide identification and characterization of wall-associated kinases, molecular docking and polysaccharide elicitation of monoterpenoid indole alkaloids in micro-propagated Catharanthus roseus. Journal of plant research. 2024 Jan; 137(1):125-142. doi: 10.1007/s10265-023-01504-1. [PMID: 37962734]
  • Zhongping Xu, Guanying Wang, Qiongqiong Wang, Xiaoting Li, Guangyu Zhang, Ali Qurban, Can Zhang, Yi Zhou, Huan Si, Lisong Hu, Fuqiu Wang, Ying Wang, Zhitao Tian, Wei Chen, Shuangxia Jin, Fang Ding. A near-complete genome assembly of Catharanthus roseus and insights into its vinblastine biosynthesis and high susceptibility to the Huanglongbing pathogen. Plant communications. 2023 Nov; 4(6):100661. doi: 10.1016/j.xplc.2023.100661. [PMID: 37464741]
  • Maneesha Mall, Karuna Shanker, Dinesh A Nagegowda, Abdul Samad, Alok Kalra, Alok Pandey, Velusamy Sundaresan, Ashutosh K Shukla. Temperature-induced lipocalin-mediated membrane integrity: Possible implications for vindoline accumulation in Catharanthus roseus leaves. Physiologia plantarum. 2023 Sep; 175(5):e13994. doi: 10.1111/ppl.13994. [PMID: 37882277]
  • Katalin Nagy, Éva Darkó, Gabriella Szalai, Tibor Janda, Zsuzsa Jókai, Márta Ladányi, Mohamed Ramadan Rady, Mihály Dernovics. UPLC-ESI-QTOF-MS assisted targeted metabolomics to study the enrichment of vinca alkaloids and related metabolites in Catharanthus roseus plants grown under controlled LED environment. Journal of pharmaceutical and biomedical analysis. 2023 Jul; 235(?):115611. doi: 10.1016/j.jpba.2023.115611. [PMID: 37542828]
  • Hossam S El-Beltagi, Salwa M El-Sayed, Ahmed N Abdelhamid, Karim M Hassan, Walaa A Elshalakany, Mona Ibrahim Nossier, Nadiyah M Alabdallah, Nadi Awad Al-Harbi, Salem Mesfir Al-Qahtani, Doaa Bahaa Eldin Darwish, Zahid Khorshid Abbas, Hemmat A Ibrahim. Potentiating Biosynthesis of Alkaloids and Polyphenolic Substances in Catharanthus roseus Plant Using ĸ-Carrageenan. Molecules (Basel, Switzerland). 2023 Apr; 28(8):. doi: 10.3390/molecules28083642. [PMID: 37110876]
  • Yuanjian Yang, Liuyu Ding, Ying Zhou, Zizheng Guo, Rongmin Yu, Jianhua Zhu. Establishment of recombinant Catharanthus roseus stem cells stably overexpressing ORCA4 for terpenoid indole alkaloids biosynthesis. Plant physiology and biochemistry : PPB. 2023 Feb; 196(?):783-792. doi: 10.1016/j.plaphy.2023.02.039. [PMID: 36848864]
  • Valentina Laghezza Masci, Davide Stefanoni, Angelo D'Alessandro, Marta Zambelli, Lorenzo Modesti, Daniele Pollini, Elisa Ovidi, Antonio Tiezzi. Induction of Drug-Resistance and Production of a Culture Medium Able to Induce Drug-Resistance in Vinblastine Untreated Murine Myeloma Cells. Molecules (Basel, Switzerland). 2023 Feb; 28(5):. doi: 10.3390/molecules28052051. [PMID: 36903299]
  • Dagny Grzech, Benke Hong, Lorenzo Caputi, Prashant D Sonawane, Sarah E O'Connor. Engineering the Biosynthesis of Late-Stage Vinblastine Precursors Precondylocarpine Acetate, Catharanthine, Tabersonine in Nicotiana benthamiana. ACS synthetic biology. 2023 01; 12(1):27-34. doi: 10.1021/acssynbio.2c00434. [PMID: 36516122]
  • Fanfan Li, Stephen Bordeleau, Kyung Hee Kim, Jonathan Turcotte, Benjamin Davis, Lan Liu, Stéphane Bayen, Vincenzo De Luca, Mehran Dastmalchi. A lesion-mimic mutant of Catharanthus roseus accumulates the opioid agonist, akuammicine. Phytochemistry. 2022 Nov; 203(?):113422. doi: 10.1016/j.phytochem.2022.113422. [PMID: 36055422]
  • M Ahmadzadeh, A H Keshtkar, K Moslemkhany, M Ahmadzadeh. Effect of the plant probiotic bacteria on terpenoid indole alkaloid biosynthesis pathway gene expression profiling, vinblastine and vincristine content in the root of Catharanthus roseus. Molecular biology reports. 2022 Nov; 49(11):10357-10365. doi: 10.1007/s11033-022-07841-z. [PMID: 36097118]
  • Armando Moreno-Velasco, Pedro de Jesús Flores-Tafoya, Mabel Fragoso-Serrano, Suzana Guimarães Leitão, Rogelio Pereda-Miranda. Resin Glycosides from Operculina hamiltonii and Their Synergism with Vinblastine in Cancer Cells. Journal of natural products. 2022 10; 85(10):2385-2394. doi: 10.1021/acs.jnatprod.2c00594. [PMID: 36162138]
  • Narges Soltani, Farhad Nazarian Firouzabadi, Alireza Shafeinia, Masoud Shirali, Ayeh Sadat Sadr. De Novo transcriptome assembly and differential expression analysis of catharanthus roseus in response to salicylic acid. Scientific reports. 2022 10; 12(1):17803. doi: 10.1038/s41598-022-20314-4. [PMID: 36280677]
  • A Mujib, Samar Fatima, Moien Qadir Malik. Cryo-derived plants through embryogenesis showed same levels of vinblastine and vincristine (anticancer) in Catharanthus roseus and had normal genome size. Scientific reports. 2022 10; 12(1):16635. doi: 10.1038/s41598-022-20993-z. [PMID: 36198853]
  • Shagufta Iqbal, Caitlin Flux, Deborah A Briggs, Evelyne Deplazes, Jiansi Long, Ruth Skrzypek, Alice Rothnie, Ian D Kerr, Richard Callaghan. Vinca alkaloid binding to P-glycoprotein occurs in a processive manner. Biochimica et biophysica acta. Biomembranes. 2022 10; 1864(10):184005. doi: 10.1016/j.bbamem.2022.184005. [PMID: 35863425]
  • Jie Zhang, Lea G Hansen, Olga Gudich, Konrad Viehrig, Lærke M M Lassen, Lars Schrübbers, Khem B Adhikari, Paulina Rubaszka, Elena Carrasquer-Alvarez, Ling Chen, Vasil D'Ambrosio, Beata Lehka, Ahmad K Haidar, Saranya Nallapareddy, Konstantina Giannakou, Marcos Laloux, Dushica Arsovska, Marcus A K Jørgensen, Leanne Jade G Chan, Mette Kristensen, Hanne B Christensen, Suresh Sudarsan, Emily A Stander, Edward Baidoo, Christopher J Petzold, Tune Wulff, Sarah E O'Connor, Vincent Courdavault, Michael K Jensen, Jay D Keasling. A microbial supply chain for production of the anti-cancer drug vinblastine. Nature. 2022 09; 609(7926):341-347. doi: 10.1038/s41586-022-05157-3. [PMID: 36045295]
  • A Mujib, Samar Fatima, Moien Qadir Malik. Gamma ray-induced tissue responses and improved secondary metabolites accumulation in Catharanthus roseus. Applied microbiology and biotechnology. 2022 Sep; 106(18):6109-6123. doi: 10.1007/s00253-022-12122-7. [PMID: 35962802]
  • Wojciech Trybus, Ewa Trybus, Teodora Król. Emodin Sensitizes Cervical Cancer Cells to Vinblastine by Inducing Apoptosis and Mitotic Death. International journal of molecular sciences. 2022 Jul; 23(15):. doi: 10.3390/ijms23158510. [PMID: 35955645]
  • Jasmine Ga May Eng, Mohammadamin Shahsavarani, Daniel Patrick Smith, Josef Hájíček, Vincenzo De Luca, Yang Qu. A Catharanthus roseus Fe(II)/α-ketoglutarate-dependent dioxygenase catalyzes a redox-neutral reaction responsible for vindolinine biosynthesis. Nature communications. 2022 06; 13(1):3335. doi: 10.1038/s41467-022-31100-1. [PMID: 35680936]
  • L T van der Heijden, A Gebretensae, B Thijssen, L van Andel, A L Nijstad, Y Wang, H Rosing, A D R Huitema, J H Beijnen. A highly sensitive bioanalytical method for the quantification of vinblastine, vincristine, vinorelbine and 4-O-deacetylvinorelbine in human plasma using LC-MS/MS. Journal of pharmaceutical and biomedical analysis. 2022 Jun; 215(?):114772. doi: 10.1016/j.jpba.2022.114772. [PMID: 35462284]
  • K Zhao, H Q Wang, L Li, T Song, S P Li, M H Qiu. [Efficacy and safety of Camrelizumab and AVD in the first-line treatment of classic Hodgkin's lymphoma]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi. 2022 05; 43(5):431-434. doi: 10.3760/cma.j.issn.0253-2727.2022.05.015. [PMID: 35680603]
  • Maneesha Mall, Karuna Shanker, Abdul Samad, Alok Kalra, Velusamy Sundaresan, Ashutosh K Shukla. Stress responsiveness of vindoline accumulation in Catharanthus roseus leaves is mediated through co-expression of allene oxide cyclase with pathway genes. Protoplasma. 2022 May; 259(3):755-773. doi: 10.1007/s00709-021-01701-6. [PMID: 34459997]
  • Vyoma Mistry, Siddhi Darji, Pragya Tiwari, Abhishek Sharma. Engineering Catharanthus roseus monoterpenoid indole alkaloid pathway in yeast. Applied microbiology and biotechnology. 2022 Apr; 106(7):2337-2347. doi: 10.1007/s00253-022-11883-5. [PMID: 35333954]
  • Wenzhu Tang, Xiaoqi Liu, Yuning He, Fan Yang. Enhancement of Vindoline and Catharanthine Accumulation, Antioxidant Enzymes Activities, and Gene Expression Levels in Catharanthus roseus Leaves by Chitooligosaccharides Elicitation. Marine drugs. 2022 Mar; 20(3):. doi: 10.3390/md20030188. [PMID: 35323487]
  • Matthew J Murray, Rafael Moleron, Jennifer Adamski, Martin English, G A Amos Burke, Justin Cross, Thankamma Ajithkumar, Sara Stoneham, James C Nicholson. Vinblastine monotherapy induction prior to radiotherapy for patients with intracranial germinoma during the COVID-19 pandemic. Pediatric blood & cancer. 2022 01; 69(1):e29359. doi: 10.1002/pbc.29359. [PMID: 34520101]
  • Tuan-Anh Minh Nguyen, Matthew McConnachie, Trinh-Don Nguyen, Thu-Thuy T Dang. Discovery and Characterization of Oxidative Enzymes Involved in Monoterpenoid Indole Alkaloid Biosynthesis. Methods in molecular biology (Clifton, N.J.). 2022; 2505(?):141-164. doi: 10.1007/978-1-0716-2349-7_11. [PMID: 35732943]
  • Zhichun Li, Liliang Ren. Study on Effects of Cyclophosphamide Combined with Vinorelbine in Advanced Small Cell Lung Cancer and Anteroposterior Changes in MRI. Contrast media & molecular imaging. 2022; 2022(?):3104879. doi: 10.1155/2022/3104879. [PMID: 36043147]
  • Mohammadamin Shahsavarani, Maisha Farzana, Vincenzo De Luca, Yang Qu. Generating an EMS Mutant Population and Rapid Mutant Screening by Thin-Layer Chromatography Enables the Studies of Monoterpenoid Indole Alkaloids Biosynthesis in Catharanthus Roseus. Methods in molecular biology (Clifton, N.J.). 2022; 2505(?):181-190. doi: 10.1007/978-1-0716-2349-7_13. [PMID: 35732945]
  • Dikki Pedenla Bomzan, H B Shilpashree, Dinesh A Nagegowda. Agrobacterium-Mediated in Planta Transformation in Periwinkle. Methods in molecular biology (Clifton, N.J.). 2022; 2505(?):301-315. doi: 10.1007/978-1-0716-2349-7_22. [PMID: 35732954]
  • Szabolcs Mayer, Nóra Nagy, Péter Keglevich, Áron Szigetvári, Miklós Dékány, Csaba Szántay Junior, László Hazai. Synthesis of Novel Vindoline-Chrysin Hybrids. Chemistry & biodiversity. 2022 Jan; 19(1):e202100725. doi: 10.1002/cbdv.202100725. [PMID: 34874114]
  • Hiroyuki Fujii, Taisuke Tsuji, Mio Sugitani, Yosuke Matsumoto, Tatsuya Yuba, Shunya Tanaka, Yoshifumi Suga, Aosa Matsuyama, Shiho Goda, Ayaka Omura, Shinsuke Shiotsu, Chieko Takumi, Seiko Ono, Noriya Hiraoka. Prolonged persistence of SARS-CoV-2 infection during A+AVD therapy for classical Hodgkin's lymphoma: A case report. Current problems in cancer. 2021 12; 45(6):100739. doi: 10.1016/j.currproblcancer.2021.100739. [PMID: 33810911]
  • E R El-Sayed. Discovery of the anticancer drug vinblastine from the endophytic Alternaria alternata and yield improvement by gamma irradiation mutagenesis. Journal of applied microbiology. 2021 Dec; 131(6):2886-2898. doi: 10.1111/jam.15169. [PMID: 34062037]
  • Stéphane Culine, Valentin Harter, Gwenaelle Gravis, Aude Fléchon, Christine Chevreau, Hakim Mahammedi, Brigitte Laguerre, Aline Guillot, Florence Joly, Sophie Abadie-Lacourtoisie, Lionnel Geoffrois, Frédéric Di Fiore, Guilhem Roubaud, Philippe Barthélémy, Eric Voog, Sheik Emambux, Camille Serrate, Carolina Saldana, Thierry Nguyen-Tan-Hon, Yohann Loriot, Jean-Christophe Eymard, Olivier Huillard, Frédéric Rolland, Nadine Houédé, Jean-Philippe Spano, Mounira El Demery, Sabine Vieillot, Tifenn L'Haridon, Werner Hilgers, Yves Allory, Christian Pfister. Chemotherapy for Muscle-invasive Bladder Cancer: Impact of Cisplatin Delivery on Renal Function and Local Control Rate in the Randomized Phase III VESPER (GETUG-AFU V05) Trial. Clinical genitourinary cancer. 2021 12; 19(6):554-562. doi: 10.1016/j.clgc.2021.08.005. [PMID: 34602349]
  • Natalja Kulagina, Grégory Guirimand, Céline Melin, Pamela Lemos-Cruz, Ines Carqueijeiro, Johan-Owen De Craene, Audrey Oudin, Vladimir Heredia, Konstantinos Koudounas, Marianne Unlubayir, Arnaud Lanoue, Nadine Imbault, Benoit St-Pierre, Nicolas Papon, Marc Clastre, Nathalie Giglioli-Guivarc'h, Jillian Marc, Sébastien Besseau, Vincent Courdavault. Enhanced bioproduction of anticancer precursor vindoline by yeast cell factories. Microbial biotechnology. 2021 11; 14(6):2693-2699. doi: 10.1111/1751-7915.13898. [PMID: 34302444]
  • Shamsher Ali, Eric Hénon, Ritchy Leroy, Georges Massiot. Addition of Vindoline to p-Benzoquinone: Regiochemistry, Stereochemistry and Symmetry Considerations. Molecules (Basel, Switzerland). 2021 Oct; 26(21):. doi: 10.3390/molecules26216395. [PMID: 34770804]
  • Oktay Perk, Tanıl Kendirli, Handan Dinçaslan, Ebru Azapağası, Gokcen Meral. Overlap Stevens Johnson Syndrome/Toxic Epidermal Necrolysis developed due to the use of toxic-dose vinblastine in case of Langerhans Cell Histiocytosis(Letterer-Siwe). Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis. 2021 Oct; 60(5):103173. doi: 10.1016/j.transci.2021.103173. [PMID: 34215518]
  • Tengfei Liu, Ying Huang, Lihong Jiang, Chang Dong, Yuanwei Gou, Jiazhang Lian. Efficient production of vindoline from tabersonine by metabolically engineered Saccharomyces cerevisiae. Communications biology. 2021 09; 4(1):1089. doi: 10.1038/s42003-021-02617-w. [PMID: 34531512]
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