Inertial focusing for tumor antigen-dependent and -independent sorting of rare circulating tumor cells.
Inertial focusing for tumor antigen-dependent and -independent sorting of rare circulating tumor cells.
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DOI:
10.1126/scitranslmed.3005616
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发表时间:
2013-04-03
影响因子:
17.1
通讯作者:
Toner M
中科院分区:
文献类型:
--
作者:
Ozkumur E;Shah AM;Ciciliano JC;Emmink BL;Miyamoto DT;Brachtel E;Yu M;Chen PI;Morgan B;Trautwein J;Kimura A;Sengupta S;Stott SL;Karabacak NM;Barber TA;Walsh JR;Smith K;Spuhler PS;Sullivan JP;Lee RJ;Ting DT;Luo X;Shaw AT;Bardia A;Sequist LV;Louis DN;Maheswaran S;Kapur R;Haber DA;Toner M
Circulating tumor cells (CTCs) are shed into the bloodstream from primary and metastatic tumor deposits. Their isolation and analysis hold great promise for the early detection of invasive cancer and the management of advanced disease, but technological hurdles have limited their broad clinical utility. We describe an inertial focusing–enhanced microfluidic CTC capture platform, termed “CTC-iChip,” that is capable of sorting rare CTCs from whole blood at 107 cells/s. Most importantly, the iChip is capable of isolating CTCs using strategies that are either dependent or independent of tumor membrane epitopes, and thus applicable to virtually all cancers. We specifically demonstrate the use of the iChip in an expanded set of both epithelial and nonepithelial cancers including lung, prostate, pancreas, breast, and melanoma. The sorting of CTCs as unfixed cells in solution allows for the application of high-quality clinically standardized morphological and immunohistochemical analyses, as well as RNA-based single-cell molecular characterization. The combination of an unbiased, broadly applicable, high-throughput, and automatable rare cell sorting technology with generally accepted molecular assays and cytology standards will enable the integration of CTC-based diagnostics into the clinical management of cancer.
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影响因子:
28.2
作者:
Miyamoto DT;Lee RJ;Stott SL;Ting DT;Wittner BS;Ulman M;Smas ME;Lord JB;Brannigan BW;Trautwein J;Bander NH;Wu CL;Sequist LV;Smith MR;Ramaswamy S;Toner M;Maheswaran S;Haber DA
通讯作者:
Haber DA
影响因子:
3
作者:
Huang, R.;Barber, T. A.;Schmidt, M. A.;Tompkins, R. G.;Toner, M.;Bianchi, D. W.;Kapur, R.;Flejter, W. L.
通讯作者:
Flejter, W. L.
DOI:
10.1186/bcr2131
发表时间:
2008
期刊:
Breast cancer research : BCR
影响因子:
--
作者:
Deng G;Herrler M;Burgess D;Manna E;Krag D;Burke JF
通讯作者:
Burke JF
影响因子:
17.1
作者:
Stott SL;Lee RJ;Nagrath S;Yu M;Miyamoto DT;Ulkus L;Inserra EJ;Ulman M;Springer S;Nakamura Z;Moore AL;Tsukrov DI;Kempner ME;Dahl DM;Wu CL;Iafrate AJ;Smith MR;Tompkins RG;Sequist LV;Toner M;Haber DA;Maheswaran S
通讯作者:
Maheswaran S
DOI:
10.1073/pnas.0404036101
发表时间:
2004-07-20
影响因子:
11.1
作者:
Krivacic, RT;Ladanyi, A;Bruce, RH
通讯作者:
Bruce, RH