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Cytotoxicity

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120:. LDH reduces NAD to NADH which elicits a colour change by interaction with a specific probe. Protease biomarkers have been identified that allow researchers to measure relative numbers of live and dead cells within the same cell population. The live-cell protease is only active in cells that have a healthy cell membrane, and loses activity once the cell is compromised and the protease is exposed to the external environment. The dead-cell protease cannot cross the cell membrane, and can only be measured in culture media after cells have lost their membrane integrity. 111:
are normally excluded from the inside of healthy cells; however, if the cell membrane has been compromised, they freely cross the membrane and stain intracellular components. Alternatively, membrane integrity can be assessed by monitoring the passage of substances that are normally sequestered inside
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Cells undergoing necrosis typically exhibit rapid swelling, lose membrane integrity, shut down metabolism, and release their contents into the environment. Cells that undergo rapid necrosis in vitro do not have sufficient time or energy to activate apoptotic machinery and will not express apoptotic
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Cytotoxicity assays are widely used by the pharmaceutical industry to screen for cytotoxicity in compound libraries. Researchers can either look for cytotoxic compounds, if they are interested in developing a therapeutic that targets rapidly dividing cancer cells, for instance; or they can screen
127:) or with 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT), which yields a water-soluble product, or the MTS assay. This assay measures the reducing potential of the cell using a colorimetric reaction. Viable cells will reduce the MTS reagent to a colored 89:
of the cell, cytoplasmic shrinkage, nuclear condensation and cleavage of DNA into regularly sized fragments. Cells in culture that are undergoing apoptosis eventually undergo secondary necrosis. They will shut down metabolism, lose membrane integrity and lyse.
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Suitable assays can be combined and performed sequentially on the same cells in order to reduce assay-specific false positive or false negative results. A possible combination is LDH-XTT-NR (Neutral red assay)-SRB which is also available in a kit format.
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contain cytotoxic drugs, whose purpose is interfering with the cell division. These drugs cannot distinguish between normal and malignant cells, but they inhibit the overall process of cell division with the purpose to kill the cancers before the hosts.
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A label-free approach to follow the cytotoxic response of adherent animal cells in real-time is based on electric impedance measurements when the cells are grown on gold-film electrodes. This technology is referred to as
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Assessing cell membrane integrity is one of the most common ways to measure cell viability and cytotoxic effects. Compounds that have cytotoxic effects often compromise cell membrane integrity. Vital dyes, such as
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Decker T, Lohmann-Matthes ML (November 1988). "A quick and simple method for the quantitation of lactate dehydrogenase release in measurements of cellular cytotoxicity and tumor necrosis factor (TNF) activity".
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Niles AL, Moravec RA, Eric Hesselberth P, Scurria MA, Daily WJ, Riss TL (July 2007). "A homogeneous assay to measure live and dead cells in the same sample by detecting different protease markers".
41:. Examples of toxic agents are toxic metals, toxic chemicals, microbe neurotoxins, radiation particles and even specific neurotransmitters when the system is out of balance. Also some types of 305:
Riss TL, Moravec RA (February 2004). "Use of multiple assay endpoints to investigate the effects of incubation time, dose of toxin, and plating density in cell-based cytotoxicity assays".
737: 166:(ECIS). Label-free real-time techniques provide the kinetics of the cytotoxic response rather than just a snapshot like many colorimetric endpoint assays. 77:. The cells can stop actively growing and dividing (a decrease in cell viability), or the cells can activate a genetic program of controlled cell death ( 135:. In addition to using dyes to indicate the redox potential of cells in order to monitor their viability, researchers have developed assays that use 619: 214: 193:
methods have been suggested. An independent comparison of these methods has been done within the "Toxicology in the 21st century" project.
99:"hits" from initial high-throughput drug screens for unwanted cytotoxic effects before investing in their development as a pharmaceutical. 117: 163: 139:
content as a marker of viability. Such ATP-based assays include bioluminescent assays in which ATP is the limiting reagent for the
562:"Cytotoxic Drug Dispersal, Cytotoxic Safety, and Cytotoxic Waste Management: Practices and Proposed India-specific Guidelines" 713: 181:
A highly important topic is the prediction of cytotoxicity of chemical compounds based on previous measurements, i.e.
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markers. Apoptosis is characterized by well defined cytological and molecular events including a change in the
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Cytotoxicity can also be monitored using 3-(4, 5-Dimethyl-2-thiazolyl)-2, 5-diphenyl-2H-tetrazolium bromide (
225:. Lymphocyte-mediated cytotoxicity, on the other hand, does not have to be mediated by antibodies; nor does 276: 503:
Easty, A.C.; Coakley, N.; Cheng, R.; Cividino, M.; Savage, P.; Tozer, R.; White, R.E. (February 2015).
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Treating cells with the cytotoxic compound can result in a variety of prognoses. The cells may undergo
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product. A similar redox-based assay has also been developed using the fluorescent dye,
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Fan F, Wood KV (February 2007). "Bioluminescent assays for high-throughput screening".
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Dearden, J. C. (2003). "In silico prediction of drug toxicity".
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Gavanji S, Bakhtari A, Famurewa AC, Othman EM (January 2023).
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Material that has been determined as cytotoxic, typically
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https://tripod.nih.gov/tox21/challenge/leaderboard.jsp
388: 217:(ADCC) describes the cell-killing ability of certain 221:, which requires the target cell being marked by an 566:Indian Journal of Medical and Paediatric Oncology 775: 683:"Toxicology in the 21st century Data Challenge" 560:Capoor, Malini R; Bhowmik, Kumar Tapas (2017). 559: 215:Antibody-dependent cell-mediated cytotoxicity 618:: CS1 maint: DOI inactive as of July 2024 ( 738:"How Is Chemotherapy Used to Treat Cancer?" 626: 304: 635:Journal of Computer-aided Molecular Design 766:at the U.S. National Library of Medicine 695: 595: 577: 536: 357: 164:electric cell-substrate impedance sensing 146:Cytotoxicity can also be measured by the 632: 459: 300: 298: 296: 14: 776: 698:Cancer Chemotherapy: an Introduction 677: 293: 112:cells to the outside. One molecule, 24: 116:(LDH), is commonly measured using 64: 25: 800: 757: 227:complement-dependent cytotoxicity 229:(CDC), which is mediated by the 209: 730: 689: 185:testing. For this purpose many 27:Quality of being toxic to cells 553: 496: 453: 418: 382: 333: 93: 13: 1: 287: 267:Antireticular Cytotoxic Serum 176: 404:10.1016/0022-1759(88)90310-9 346:Chemistry & Biodiversity 277:Membrane vesicle trafficking 7: 260: 150:(SRB) assay, WST assay and 10: 805: 579:10.4103/ijmpo.ijmpo_174_16 319:10.1089/154065804322966315 236:Three groups of cytotoxic 196: 706:10.1007/978-1-4471-1686-8 696:Priestman, T. J. (1989). 272:Host–pathogen interaction 768:Medical Subject Headings 439:10.1016/j.ab.2007.04.007 33:is the quality of being 655:10.1023/A:1025361621494 582:(inactive 2024-07-11). 462:Assay Drug Dev Technol 359:10.1002/cbdv.202201098 307:Assay Drug Dev Technol 255:Natural killer T cells 61:) are toxic to cells. 114:lactate dehydrogenase 474:10.1089/adt.2006.053 250:Natural killer cells 55:brown recluse spider 647:2003JCAMD..17..119D 392:J. Immunol. Methods 240:are distinguished: 521:10.3747/co.21.2151 59:Loxosceles reclusa 715:978-3-540-19551-1 245:Cytotoxic T cells 231:complement system 191:virtual screening 16:(Redirected from 796: 752: 751: 749: 748: 734: 728: 727: 693: 687: 681: 675: 674: 641:(2–4): 119–127. 630: 624: 623: 617: 609: 599: 581: 557: 551: 550: 540: 509:Current Oncology 500: 494: 493: 457: 451: 450: 422: 416: 415: 386: 380: 379: 361: 337: 331: 330: 302: 171:biomedical waste 152:clonogenic assay 148:sulforhodamine B 109:propidium iodide 87:refractive index 45:, e.g. from the 21: 804: 803: 799: 798: 797: 795: 794: 793: 774: 773: 760: 755: 746: 744: 736: 735: 731: 716: 694: 690: 682: 678: 631: 627: 611: 610: 558: 554: 501: 497: 458: 454: 423: 419: 387: 383: 338: 334: 303: 294: 290: 263: 212: 199: 179: 96: 67: 65:Cell physiology 28: 23: 22: 15: 12: 11: 5: 802: 792: 791: 786: 772: 771: 759: 758:External links 756: 754: 753: 742:www.cancer.org 729: 714: 688: 676: 625: 572:(2): 190–197. 552: 515:(1): e27–e37. 495: 452: 433:(2): 197–206. 417: 381: 332: 291: 289: 286: 285: 284: 279: 274: 269: 262: 259: 258: 257: 252: 247: 211: 208: 203:chemotherapies 198: 195: 178: 175: 95: 92: 66: 63: 51:Bitis arietans 26: 9: 6: 4: 3: 2: 801: 790: 787: 785: 782: 781: 779: 769: 765: 762: 761: 743: 739: 733: 725: 721: 717: 711: 707: 703: 699: 692: 686: 680: 672: 668: 664: 660: 656: 652: 648: 644: 640: 636: 629: 621: 615: 607: 603: 598: 593: 589: 585: 580: 575: 571: 567: 563: 556: 548: 544: 539: 534: 530: 526: 522: 518: 514: 510: 506: 499: 491: 487: 483: 479: 475: 471: 468:(1): 127–36. 467: 463: 456: 448: 444: 440: 436: 432: 428: 427:Anal. Biochem 421: 413: 409: 405: 401: 397: 393: 385: 377: 373: 369: 365: 360: 355: 351: 347: 343: 336: 328: 324: 320: 316: 312: 308: 301: 299: 297: 292: 283: 280: 278: 275: 273: 270: 268: 265: 264: 256: 253: 251: 248: 246: 243: 242: 241: 239: 234: 232: 228: 224: 220: 216: 210:Immune system 207: 204: 194: 192: 188: 184: 174: 172: 167: 165: 159: 155: 153: 149: 144: 142: 138: 134: 130: 126: 121: 119: 115: 110: 106: 100: 91: 88: 82: 80: 76: 72: 62: 60: 56: 52: 48: 44: 40: 36: 32: 19: 745:. Retrieved 741: 732: 697: 691: 679: 638: 634: 628: 614:cite journal 569: 565: 555: 512: 508: 498: 465: 461: 455: 430: 426: 420: 395: 391: 384: 349: 345: 335: 313:(1): 51–62. 310: 306: 282:Snake toxins 235: 213: 200: 180: 168: 160: 156: 145: 122: 101: 97: 83: 68: 58: 50: 31:Cytotoxicity 30: 29: 398:(1): 61–9. 352:(2): 3–27. 238:lymphocytes 219:lymphocytes 105:trypan blue 94:Measurement 789:Immunology 784:Toxicology 778:Categories 764:Cytotoxins 747:2021-06-28 288:References 177:Prediction 143:reaction. 141:luciferase 75:cell lysis 47:puff adder 588:0971-5851 529:1198-0052 376:255473013 183:in-silico 133:resazurin 118:LDH assay 79:apoptosis 18:Cytotoxic 724:20058092 671:21518449 663:13677480 606:28900329 547:25684994 490:10261888 482:17355205 447:17512890 368:36595710 327:15090210 261:See also 223:antibody 129:formazan 71:necrosis 643:Bibcode 597:5582558 538:4324350 412:3192948 197:Cancers 770:(MeSH) 722:  712:  669:  661:  604:  594:  586:  545:  535:  527:  488:  480:  445:  410:  374:  366:  325:  720:S2CID 667:S2CID 486:S2CID 372:S2CID 201:Some 53:) or 43:venom 39:cells 35:toxic 710:ISBN 659:PMID 620:link 602:PMID 584:ISSN 543:PMID 525:ISSN 478:PMID 443:PMID 408:PMID 364:PMID 323:PMID 189:and 187:QSAR 702:doi 651:doi 592:PMC 574:doi 533:PMC 517:doi 470:doi 435:doi 431:366 400:doi 396:115 354:doi 315:doi 137:ATP 125:MTT 107:or 81:). 37:to 780:: 740:. 718:. 708:. 700:. 665:. 657:. 649:. 639:17 637:. 616:}} 612:{{ 600:. 590:. 570:38 568:. 564:. 541:. 531:. 523:. 513:22 511:. 507:. 484:. 476:. 464:. 441:. 429:. 406:. 394:. 370:. 362:. 350:20 348:. 344:. 321:. 309:. 295:^ 233:. 154:. 750:. 726:. 704:: 673:. 653:: 645:: 622:) 608:. 576:: 549:. 519:: 492:. 472:: 466:5 449:. 437:: 414:. 402:: 378:. 356:: 329:. 317:: 311:2 57:( 49:( 20:)

Index

Cytotoxic
toxic
cells
venom
puff adder
brown recluse spider
necrosis
cell lysis
apoptosis
refractive index
trypan blue
propidium iodide
lactate dehydrogenase
LDH assay
MTT
formazan
resazurin
ATP
luciferase
sulforhodamine B
clonogenic assay
electric cell-substrate impedance sensing
biomedical waste
in-silico
QSAR
virtual screening
chemotherapies
Antibody-dependent cell-mediated cytotoxicity
lymphocytes
antibody

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