2013
DOI: 10.1038/aja.2013.106
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Investigating intratumour heterogeneity by single-cell sequencing

Abstract: Intratumour heterogeneity is a longstanding field of focus for both researchers and clinicians. It refers to the diversity amongst cells within the same tumour. Two major hypotheses have attempted to explain the existence of intratumour heterogeneity: (i) the clonal evolution (CE) theory and (ii) the cancer stem cell (CSC) model. CE theory emphasizes the evolutionary biological characteristics of the tumour, underscoring the initiation and progression of the disease. In contrast, the CSC model focuses on stem … Show more

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Cited by 18 publications
(13 citation statements)
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“…[ 3 ] who proposed the concept of branched evolutionary tumor growth. Our dynamic study in a living patient reinforces this concept and the clonal evolution theory [ 6 , 7 ]. However, the fact that we identified a minority TP53 -mutated clone in the primary tumor later expanded in the metastasis suggests that molecular abnormalities responsible for the metastatic process are usually not highlighted by whole tissue analyses of primary tumors.…”
Section: Discussionsupporting
confidence: 80%
See 1 more Smart Citation
“…[ 3 ] who proposed the concept of branched evolutionary tumor growth. Our dynamic study in a living patient reinforces this concept and the clonal evolution theory [ 6 , 7 ]. However, the fact that we identified a minority TP53 -mutated clone in the primary tumor later expanded in the metastasis suggests that molecular abnormalities responsible for the metastatic process are usually not highlighted by whole tissue analyses of primary tumors.…”
Section: Discussionsupporting
confidence: 80%
“…According to the clonal evolution model, oncogenic selection increases the phenotypic and genotypic heterogeneity of cancer cells within tumors [ 6 , 7 ]. A malignant tumor is composed of sub-clones, and additional mutations can occur during evolution [ 8 ].…”
Section: Introductionmentioning
confidence: 99%
“…Single-cell genomic sequencing or single nuclear genome sequencing is useful to study mutations, single nucleotide variations, and indels (insertion and deletions) [ 50 ] . Multiple methods of SCS for single nuclear genome have been designed [ Table 1 ].…”
Section: Single-cell Sequencing: a Promising Tool For Deciphering Tummentioning
confidence: 99%
“…Prostate cancer is a kind of heterogeneous cancer with different phenotypes and outcomes 81. Most PCa present to be indolent with mild and atypical clinical manifestations, which may confuse and mislead clinicians and patients at the point of disease diagnosis.…”
Section: Conclusion and Prospectivementioning
confidence: 99%