» Articles » PMID: 27189371

Minimal Residual Disease in Breast Cancer: an Overview of Circulating and Disseminated Tumour Cells

Overview
Specialty Oncology
Date 2016 May 19
PMID 27189371
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

Within the field of cancer research, focus on the study of minimal residual disease (MRD) in the context of carcinoma has grown exponentially over the past several years. MRD encompasses circulating tumour cells (CTCs)-cancer cells on the move via the circulatory or lymphatic system, disseminated tumour cells (DTCs)-cancer cells which have escaped into a distant site (most studies have focused on bone marrow), and resistant cancer cells surviving therapy-be they local or distant, all of which may ultimately give rise to local relapse or overt metastasis. Initial studies simply recorded the presence and number of CTCs and DTCs; however recent advances are allowing assessment of the relationship between their persistence, patient prognosis and the biological properties of MRD, leading to a better understanding of the metastatic process. Technological developments for the isolation and analysis of circulating and disseminated tumour cells continue to emerge, creating new opportunities to monitor disease progression and perhaps alter disease outcome. This review outlines our knowledge to date on both measurement and categorisation of MRD in the form of CTCs and DTCs with respect to how this relates to cancer outcomes, and the hurdles and future of research into both CTCs and DTCs.

Citing Articles

Cellular residual disease (CRD) in early breast cancer -Expanding the concept of minimal residual disease monitoring?.

Serafini M, Molteni E, Nicolo E, Gerratana L, Reduzzi C, Cristofanilli M J Liq Biopsy. 2025; 3:100132.

PMID: 40026561 PMC: 11863885. DOI: 10.1016/j.jlb.2023.100132.


Adjuvant nivolumab, capecitabine or the combination in patients with residual triple-negative breast cancer: the OXEL randomized phase II study.

Lynce F, Mainor C, Donahue R, Geng X, Jones G, Schlam I Nat Commun. 2024; 15(1):2691.

PMID: 38538574 PMC: 10973408. DOI: 10.1038/s41467-024-46961-x.


Inhaled anesthesia associated with reduced mortality in patients with stage III breast cancer: A population-based study.

Kuo E, Kuo C, Lin C PLoS One. 2024; 19(3):e0289519.

PMID: 38427628 PMC: 10906904. DOI: 10.1371/journal.pone.0289519.


Tumor-derived cell-free DNA and circulating tumor cells: partners or rivals in metastasis formation?.

Witz A, Dardare J, Betz M, Gilson P, Merlin J, Harle A Clin Exp Med. 2024; 24(1):2.

PMID: 38231464 PMC: 10794481. DOI: 10.1007/s10238-023-01278-9.


Cellular Dormancy in Cancer: Mechanisms and Potential Targeting Strategies.

Min H, Lee H Cancer Res Treat. 2023; 55(3):720-736.

PMID: 36960624 PMC: 10372609. DOI: 10.4143/crt.2023.468.


References
1.
Pantel K, Alix-Panabieres C . Circulating tumour cells in cancer patients: challenges and perspectives. Trends Mol Med. 2010; 16(9):398-406. DOI: 10.1016/j.molmed.2010.07.001. View

2.
Gao D, Joshi N, Choi H, Ryu S, Hahn M, Catena R . Myeloid progenitor cells in the premetastatic lung promote metastases by inducing mesenchymal to epithelial transition. Cancer Res. 2012; 72(6):1384-94. PMC: 8543151. DOI: 10.1158/0008-5472.CAN-11-2905. View

3.
Gupta P, Chaffer C, Weinberg R . Cancer stem cells: mirage or reality?. Nat Med. 2009; 15(9):1010-2. DOI: 10.1038/nm0909-1010. View

4.
Borst P . Cancer drug pan-resistance: pumps, cancer stem cells, quiescence, epithelial to mesenchymal transition, blocked cell death pathways, persisters or what?. Open Biol. 2012; 2(5):120066. PMC: 3376736. DOI: 10.1098/rsob.120066. View

5.
Szakacs G, Paterson J, Ludwig J, Booth-Genthe C, Gottesman M . Targeting multidrug resistance in cancer. Nat Rev Drug Discov. 2006; 5(3):219-34. DOI: 10.1038/nrd1984. View