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Clonal evolution in cancer

Jesse J. Salk
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The article was published on 2010-01-01 and is currently open access. It has received 817 citations till now. The article focuses on the topics: Somatic evolution in cancer & Cancer.

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Citations
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Metastatic colonization by circulating tumour cells

TL;DR: An improved understanding of the mechanistic determinants of such colonization is needed to better prevent and treat metastatic cancer.
Journal Article

The evolutionary history of lethal metastatic prostate cancer

TL;DR: Using whole-genome sequencing, multiple metastases arising from prostate tumours in ten patients are characterized and the complex patterns of metastatic spread are elucidate in detail and the development of resistance to androgen-deprivation therapy in prostate cancer is understood.
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Clonal evolution in breast cancer revealed by single nucleus genome sequencing

TL;DR: The data show that aneuploid rearrangements occurred early in tumour evolution and remained highly stable as the tumour masses clonally expanded, which has important implications for the diagnosis, therapeutic treatment and evolution of chemoresistance in breast cancer.
References
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Genomics of Cancer and a New Era for Cancer Prevention.

TL;DR: The potential for these techniques to identify cancers at an earlier and more treatable stage using screening or other early detection approaches based on prediagnostic biospecimens is large, and their successful outcome will depend on international collaboration and planning similar to that of recent sequencing initiatives.
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Statistical Molecule Counting in Super-Resolution Fluorescence Microscopy: Towards Quantitative Nanoscopy

TL;DR: In this article, a hidden Markov model is proposed to estimate the number of fluorescent markers in a statistically meaningful manner from the raw data generated by single-marker-switching (SMS) microscopy.
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Adaptive response of resistant cancer cells to chemotherapy

TL;DR: The mechanistic studies investigating the three major components of the adaptive response, autophagy, endoplasmic reticulum (ER) stress signaling, and senescence, in response to cancer chemotherapy are summarized.