A Laboratory-Friendly CTC Identification: Comparable Double-Immunocytochemistry with Triple-Immunofluorescence.

CTC immunocytochemistry laboratory-friendly parallel double-detection

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
10 Jun 2022
Historique:
received: 25 05 2022
revised: 03 06 2022
accepted: 05 06 2022
entrez: 24 6 2022
pubmed: 25 6 2022
medline: 25 6 2022
Statut: epublish

Résumé

The source of circulating tumor cells (CTC) in the peripheral blood of patients with solid tumors are from primary cancer, metastatic sites, and a disseminated tumor cell pool. As 90% of cancer-related deaths are caused by metastatic progression and/or resistance-associated treatment failure, the above fact justifies the undeniable predictive and prognostic value of identifying CTC in the bloodstream at stages of the disease progression and resistance to treatment. Yet enumeration of CTC remains far from a standard routine procedure either for post-surgery follow-ups or ongoing adjuvant therapy. The most compelling explanation for this paradox is the absence of a convenient, laboratory-friendly, and cost-effective method to determine CTC. We presented a specific and sensitive laboratory-friendly

Identifiants

pubmed: 35740537
pii: cancers14122871
doi: 10.3390/cancers14122871
pmc: PMC9221448
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Avera McKennan Hospital & University Health Center
ID : NA

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Auteurs

Raed Sulaiman (R)

Physicians Laboratory, Department of Pathology, Avera McKennan Hospital & University Health Center, Sioux Falls, SD 57105, USA.

Pradip De (P)

Translational Oncology Laboratory, Avera Research Institute, Sioux Falls, SD 57105, USA.
Department of Internal Medicine, University of South Dakota SSOM, USD, Sioux Falls, SD 57105, USA.

Jennifer C Aske (JC)

Translational Oncology Laboratory, Avera Research Institute, Sioux Falls, SD 57105, USA.

Xiaoqian Lin (X)

Translational Oncology Laboratory, Avera Research Institute, Sioux Falls, SD 57105, USA.

Adam Dale (A)

Translational Oncology Laboratory, Avera Research Institute, Sioux Falls, SD 57105, USA.

Ethan Vaselaar (E)

Translational Oncology Laboratory, Avera Research Institute, Sioux Falls, SD 57105, USA.

Nischal Koirala (N)

Translational Oncology Laboratory, Avera Research Institute, Sioux Falls, SD 57105, USA.

Cheryl Ageton (C)

Department of Research Oncology, Clinical Research, Sioux Falls, SD 57105, USA.

Kris Gaster (K)

Avera Cancer Institute, Avera McKennan Hospital, Sioux Falls, SD 57105, USA.

Joshua Plorde (J)

Diagnostic Radiology, Interventional Radiology, and Radiology, Avera Medical Group Radiology, Sioux Falls, SD 57105, USA.

Benjamin Solomon (B)

Hematology and Oncology, Avera Medical Group Oncology & Hematology, Sioux Falls, SD 57105, USA.

Bradley Thaemert (B)

Bariatrics, Surgery, and General Surgery, Surgical Institute of South Dakota, Sioux Falls, SD 57105, USA.

Paul Meyer (P)

Cardiovascular/Thoracic Surgery, Surgery North Central Heart, A Division of Avera Heart Hospital, Sioux Falls, SD 57105, USA.

Luis Rojas Espaillat (LR)

Department of Gynecologic Oncology, Avera Cancer Institute, Sioux Falls, SD 57105, USA.

David Starks (D)

Department of Gynecologic Oncology, Avera Cancer Institute, Sioux Falls, SD 57105, USA.

Nandini Dey (N)

Translational Oncology Laboratory, Avera Research Institute, Sioux Falls, SD 57105, USA.
Department of Internal Medicine, University of South Dakota SSOM, USD, Sioux Falls, SD 57105, USA.

Classifications MeSH