Knowledge (XXG)

Cytotoxicity

Source đź“ť

109:. 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. 100:
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
73:
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
87:
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
116:) 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 78:
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.
146:
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.
194:
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.
150:
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
91:
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
378:
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".
414:
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".
30:. 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 294:
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".
726: 608: 203: 155:(ECIS). Label-free real-time techniques provide the kinetics of the cytotoxic response rather than just a snapshot like many colorimetric endpoint assays. 66:. 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 ( 152: 124:. In addition to using dyes to indicate the redox potential of cells in order to monitor their viability, researchers have developed assays that use 702: 182:
methods have been suggested. An independent comparison of these methods has been done within the "Toxicology in the 21st century" project.
88:"hits" from initial high-throughput drug screens for unwanted cytotoxic effects before investing in their development as a pharmaceutical. 215: 128:
content as a marker of viability. Such ATP-based assays include bioluminescent assays in which ATP is the limiting reagent for the
551:"Cytotoxic Drug Dispersal, Cytotoxic Safety, and Cytotoxic Waste Management: Practices and Proposed India-specific Guidelines" 260: 255: 265: 170:
A highly important topic is the prediction of cytotoxicity of chemical compounds based on previous measurements, i.e.
756: 74:
markers. Apoptosis is characterized by well defined cytological and molecular events including a change in the
112:
Cytotoxicity can also be monitored using 3-(4, 5-Dimethyl-2-thiazolyl)-2, 5-diphenyl-2H-tetrazolium bromide (
214:. Lymphocyte-mediated cytotoxicity, on the other hand, does not have to be mediated by antibodies; nor does 125: 602: 243: 102: 492:
Easty, A.C.; Coakley, N.; Cheng, R.; Cividino, M.; Savage, P.; Tozer, R.; White, R.E. (February 2015).
58:
Treating cells with the cytotoxic compound can result in a variety of prognoses. The cells may undergo
631: 43: 777: 772: 238: 708: 655: 474: 360: 106: 698: 647: 590: 572: 531: 513: 466: 431: 396: 352: 311: 219: 179: 690: 639: 580: 562: 521: 505: 458: 423: 388: 342: 303: 233: 159: 140: 136: 97: 75: 673: 162:, is often marked with a symbol that consists of a capital letter "C" inside a triangle. 635: 120:
product. A similar redox-based assay has also been developed using the fluorescent dye,
585: 550: 526: 493: 449:
Fan F, Wood KV (February 2007). "Bioluminescent assays for high-throughput screening".
191: 35: 27: 752: 766: 392: 364: 712: 659: 478: 270: 93: 567: 307: 694: 643: 226: 207: 129: 63: 576: 517: 427: 171: 121: 113: 67: 651: 594: 535: 470: 435: 356: 347: 330: 315: 400: 462: 211: 117: 59: 23: 509: 331:"Cytotoxic Activity of Herbal Medicines as Assessed in Vitro: A Review" 62:, in which they lose membrane integrity and die rapidly as a result of 31: 622:
Dearden, J. C. (2003). "In silico prediction of drug toxicity".
175: 329:
Gavanji S, Bakhtari A, Famurewa AC, Othman EM (January 2023).
158:
Material that has been determined as cytotoxic, typically
494:"Safe handling of cytotoxics: guideline recommendations" 674:
https://tripod.nih.gov/tox21/challenge/leaderboard.jsp
206:(ADCC) describes the cell-killing ability of certain 210:, which requires the target cell being marked by an 555:Indian Journal of Medical and Paediatric Oncology 672:"Toxicology in the 21st century Data Challenge" 549:Capoor, Malini R; Bhowmik, Kumar Tapas (2017). 204:Antibody-dependent cell-mediated cytotoxicity 8: 607:: CS1 maint: DOI inactive as of July 2024 ( 727:"How Is Chemotherapy Used to Treat Cancer?" 624:Journal of Computer-aided Molecular Design 755:at the U.S. National Library of Medicine 584: 566: 525: 346: 153:electric cell-substrate impedance sensing 135:Cytotoxicity can also be measured by the 289: 287: 285: 281: 600: 7: 687:Cancer Chemotherapy: an Introduction 101:cells to the outside. One molecule, 105:(LDH), is commonly measured using 14: 216:complement-dependent cytotoxicity 218:(CDC), which is mediated by the 174:testing. For this purpose many 16:Quality of being toxic to cells 1: 256:Antireticular Cytotoxic Serum 393:10.1016/0022-1759(88)90310-9 335:Chemistry & Biodiversity 266:Membrane vesicle trafficking 139:(SRB) assay, WST assay and 794: 568:10.4103/ijmpo.ijmpo_174_16 308:10.1089/154065804322966315 225:Three groups of cytotoxic 695:10.1007/978-1-4471-1686-8 685:Priestman, T. J. (1989). 261:Host–pathogen interaction 757:Medical Subject Headings 428:10.1016/j.ab.2007.04.007 22:is the quality of being 644:10.1023/A:1025361621494 571:(inactive 2024-07-11). 451:Assay Drug Dev Technol 348:10.1002/cbdv.202201098 296:Assay Drug Dev Technol 244:Natural killer T cells 50:) are toxic to cells. 103:lactate dehydrogenase 463:10.1089/adt.2006.053 239:Natural killer cells 44:brown recluse spider 636:2003JCAMD..17..119D 381:J. Immunol. Methods 229:are distinguished: 510:10.3747/co.21.2151 48:Loxosceles reclusa 704:978-3-540-19551-1 234:Cytotoxic T cells 220:complement system 180:virtual screening 785: 741: 740: 738: 737: 723: 717: 716: 682: 676: 670: 664: 663: 630:(2–4): 119–127. 619: 613: 612: 606: 598: 588: 570: 546: 540: 539: 529: 498:Current Oncology 489: 483: 482: 446: 440: 439: 411: 405: 404: 375: 369: 368: 350: 326: 320: 319: 291: 160:biomedical waste 141:clonogenic assay 137:sulforhodamine B 98:propidium iodide 76:refractive index 34:, e.g. from the 793: 792: 788: 787: 786: 784: 783: 782: 763: 762: 749: 744: 735: 733: 725: 724: 720: 705: 684: 683: 679: 671: 667: 621: 620: 616: 599: 548: 547: 543: 491: 490: 486: 448: 447: 443: 413: 412: 408: 377: 376: 372: 328: 327: 323: 293: 292: 283: 279: 252: 201: 188: 168: 85: 56: 54:Cell physiology 17: 12: 11: 5: 791: 789: 781: 780: 775: 765: 764: 761: 760: 748: 747:External links 745: 743: 742: 731:www.cancer.org 718: 703: 677: 665: 614: 561:(2): 190–197. 541: 504:(1): e27–e37. 484: 441: 422:(2): 197–206. 406: 370: 321: 280: 278: 275: 274: 273: 268: 263: 258: 251: 248: 247: 246: 241: 236: 200: 197: 192:chemotherapies 187: 184: 167: 164: 84: 81: 55: 52: 40:Bitis arietans 15: 13: 10: 9: 6: 4: 3: 2: 790: 779: 776: 774: 771: 770: 768: 758: 754: 751: 750: 746: 732: 728: 722: 719: 714: 710: 706: 700: 696: 692: 688: 681: 678: 675: 669: 666: 661: 657: 653: 649: 645: 641: 637: 633: 629: 625: 618: 615: 610: 604: 596: 592: 587: 582: 578: 574: 569: 564: 560: 556: 552: 545: 542: 537: 533: 528: 523: 519: 515: 511: 507: 503: 499: 495: 488: 485: 480: 476: 472: 468: 464: 460: 457:(1): 127–36. 456: 452: 445: 442: 437: 433: 429: 425: 421: 417: 416:Anal. Biochem 410: 407: 402: 398: 394: 390: 386: 382: 374: 371: 366: 362: 358: 354: 349: 344: 340: 336: 332: 325: 322: 317: 313: 309: 305: 301: 297: 290: 288: 286: 282: 276: 272: 269: 267: 264: 262: 259: 257: 254: 253: 249: 245: 242: 240: 237: 235: 232: 231: 230: 228: 223: 221: 217: 213: 209: 205: 199:Immune system 198: 196: 193: 185: 183: 181: 177: 173: 165: 163: 161: 156: 154: 148: 144: 142: 138: 133: 131: 127: 123: 119: 115: 110: 108: 104: 99: 95: 89: 82: 80: 77: 71: 69: 65: 61: 53: 51: 49: 45: 41: 37: 33: 29: 25: 21: 734:. Retrieved 730: 721: 686: 680: 668: 627: 623: 617: 603:cite journal 558: 554: 544: 501: 497: 487: 454: 450: 444: 419: 415: 409: 384: 380: 373: 338: 334: 324: 302:(1): 51–62. 299: 295: 271:Snake toxins 224: 202: 189: 169: 157: 149: 145: 134: 111: 90: 86: 72: 57: 47: 39: 20:Cytotoxicity 19: 18: 387:(1): 61–9. 341:(2): 3–27. 227:lymphocytes 208:lymphocytes 94:trypan blue 83:Measurement 778:Immunology 773:Toxicology 767:Categories 753:Cytotoxins 736:2021-06-28 277:References 166:Prediction 132:reaction. 130:luciferase 64:cell lysis 36:puff adder 577:0971-5851 518:1198-0052 365:255473013 172:in-silico 122:resazurin 107:LDH assay 68:apoptosis 713:20058092 660:21518449 652:13677480 595:28900329 536:25684994 479:10261888 471:17355205 436:17512890 357:36595710 316:15090210 250:See also 212:antibody 118:formazan 60:necrosis 632:Bibcode 586:5582558 527:4324350 401:3192948 186:Cancers 759:(MeSH) 711:  701:  658:  650:  593:  583:  575:  534:  524:  516:  477:  469:  434:  399:  363:  355:  314:  709:S2CID 656:S2CID 475:S2CID 361:S2CID 190:Some 42:) or 32:venom 28:cells 24:toxic 699:ISBN 648:PMID 609:link 591:PMID 573:ISSN 532:PMID 514:ISSN 467:PMID 432:PMID 397:PMID 353:PMID 312:PMID 178:and 176:QSAR 691:doi 640:doi 581:PMC 563:doi 522:PMC 506:doi 459:doi 424:doi 420:366 389:doi 385:115 343:doi 304:doi 126:ATP 114:MTT 96:or 70:). 26:to 769:: 729:. 707:. 697:. 689:. 654:. 646:. 638:. 628:17 626:. 605:}} 601:{{ 589:. 579:. 559:38 557:. 553:. 530:. 520:. 512:. 502:22 500:. 496:. 473:. 465:. 453:. 430:. 418:. 395:. 383:. 359:. 351:. 339:20 337:. 333:. 310:. 298:. 284:^ 222:. 143:. 739:. 715:. 693:: 662:. 642:: 634:: 611:) 597:. 565:: 538:. 508:: 481:. 461:: 455:5 438:. 426:: 403:. 391:: 367:. 345:: 318:. 306:: 300:2 46:( 38:(

Index

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
complement-dependent cytotoxicity

Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.

↑