Evidence map›Paper›PMID 25622539›Full record

ReviewProstate cancer and prostatic diseases2015

Re-purposing cryoablation: a combinatorial 'therapy' for the destruction of tissue.

J G Baust, J C Bischof, S Jiang-Hughes, T J Polascik, D B Rukstalis, A A Gage, J M Baust

Abstract readReview
PubMed Publisher
In one paragraph

Review in Prostate cancer and prostatic diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.0field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 48 citations in OpenAlex.

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  18. Cryoablation: physical and molecular basis with putative immunological consequences.International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group · 2019
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 6 institutions in 1 country.

J G Baust1] Institute of Biomedical Technology, State University of New York at Binghamton, Binghamton, NY, USA [2] Department of Biological Sciences, Binghamton University, Binghamton, NY, USA.
J C BischofDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, USA.
S Jiang-HughesDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, USA.
T J PolascikDivision of Urology, Department of Surgery, Duke University Medical Center, Durham, NC, USA.
D B RukstalisDepartment of Urology, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
A A GageDepartment of Surgery, State University of New York at Buffalo, Medical School, Buffalo, NY, USA.
J M BaustCPSI Biotech, Owego, NY, USA.
University of Minnesota · USBinghamton University · USCell Preservation Services (United States) · USDuke Medical Center · USUniversity at Buffalo, State University of New York · USWake Forest University · US

Funding

FrostBite - A Unique Catheter for Endoscopic CryoablationR44CA183265 · NCI · CELL PRESERVATION SERVICES, INC. · PI BAUST, JOHN M · 2017 to 2019
$1.7M
FrostBite - A Unique Catheter for Endoscopic CryoablationR43CA183265 · NCI · CELL PRESERVATION SERVICES, INC. · PI BAUST, JOHN M · 2014 to 2014
$225k
NCI NIH HHS R43 CA183265NCI NIH HHS R44 CA183265
6 · The paper itself

Abstract

It is now recognized that the tumor microenvironment creates a protective neo-tissue that isolates the tumor from the various defense strategies of the body. Evidence demonstrates that, with successive therapeutic attempts, cancer cells acquire resistance to individual treatment modalities. For example, exposure to cytotoxic drugs results in the survival of approximately 20-30% of the cancer cells as only dividing cells succumb to each toxic exposure. With follow-up treatments, each additional dose results in tumor-associated fibroblasts secreting surface-protective proteins, which enhance cancer cell resistance. Similar outcomes are reported following radiotherapy. These defensive strategies are indicative of evolved capabilities of cancer to assure successful tumor growth through well-established anti-tumor-protective adaptations. As such, successful cancer management requires the activation of multiple cellular 'kill switches' to prevent initiation of diverse protective adaptations. Thermal therapies are unique treatment modalities typically applied as monotherapies (without repetition) thereby denying cancer cells the opportunity to express defensive mutations. Further, the destructive mechanisms of action involved with cryoablation (CA) include both physical and molecular insults resulting in the disruption of multiple defensive strategies that are not cell cycle dependent and adds a damaging structural (physical) element. This review discusses the application and clinical outcomes of CA with an emphasis on the mechanisms of cell death induced by structural, metabolic, vascular and immune processes. The induction of diverse cell death cascades, resulting in the activation of apoptosis and necrosis, allows CA to be characterized as a combinatorial treatment modality. Our understanding of these mechanisms now supports adjunctive therapies that can augment cell death pathways.

Indexed as

Antineoplastic AgentsApoptosisCombined Modality TherapyCryosurgeryHumansMaleProstatic NeoplasmsSignal TransductionTumor MicroenvironmentAntineoplastic Agents

Identifiers

PMID25622539
OpenAlexW2084758592

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.