2016
DOI: 10.1038/nbt.3674
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A community-based model of rapid autopsy in end-stage cancer patients

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Cited by 71 publications
(82 citation statements)
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References 28 publications
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“…Publications on posthumous tissue collection programs are increasing in popularity, [5, 6] but to our knowledge, none have discussed the donors perceptions about participating in such programs. Improved understanding of their perceptions could lead to greater gains in knowledge, increase enrollment of patients, allow more centers to create RTD programs, and potentially allow consortia of RTD centers.…”
Section: Introductionmentioning
confidence: 99%
“…Publications on posthumous tissue collection programs are increasing in popularity, [5, 6] but to our knowledge, none have discussed the donors perceptions about participating in such programs. Improved understanding of their perceptions could lead to greater gains in knowledge, increase enrollment of patients, allow more centers to create RTD programs, and potentially allow consortia of RTD centers.…”
Section: Introductionmentioning
confidence: 99%
“…Two particular lines, MDA PCa 118a and MDA PCa 118b, were established as sub-cutaneous PDXs, providing a unique model of androgen-independent prostate cancer that induces a robust osteoblastic reaction in bone-like matrix and soft tissue [30]. Much more progress has been achieved through the recent utilisation of warm autopsy specimens, although the take rate from postmortem specimens is less than that of palliative metastatic lesions, such as those used by the Vessella group [22]. In Australia, an oncology collaboration established a warm autopsy programme to collect specimens from men who failed contemporary treatments.…”
mentioning
confidence: 98%
“…However, even for these samples, the take rate is still only 25-30 % [22]. The sources of tissue vary considerably with this subsequently affecting the quality of the specimens used for engraftment.…”
mentioning
confidence: 99%
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“…Additionally, a better understanding of the molecular function of mutant ARs is required to achieve maximal patient benefit. The field has traditionally been limited by a scarcity of CRPC models for studying AR mutant function, but new models derived from patient metastases and CTCs, such as patient-derived xenografts and organoids, are emerging (Gao et al 2014, Alsop et al 2016. As these models encompass the diversity of disease and AR alterations, they are likely to have a profound impact on our knowledge of aberrant AR signaling.…”
Section: Gata2 Oct1mentioning
confidence: 99%