Evidence map›Paper›PMID 27179759›Full record

ArticleJournal of experimental & clinical cancer research : CR2016

Transfer of malignant trait to BRCA1 deficient human fibroblasts following exposure to serum of cancer patients.

Dana Hamam, Mohamed Abdouh, Zu-Hua Gao, Vincenzo Arena, Manuel Arena, Goffredo Orazio Arena

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 42 citations in OpenAlex.

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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

6 authors at 4 institutions in 2 countries.

Dana HamamCancer Research Program, McGill University Health Centre-Research Institute, 1001 Decarie Boulevard, Montreal, H4A 3J1, QC, Canada.
Mohamed AbdouhCancer Research Program, McGill University Health Centre-Research Institute, 1001 Decarie Boulevard, Montreal, H4A 3J1, QC, Canada.
Zu-Hua GaoDepartment of Pathology, McGill University Health Centre-Research Institute, 1001 Decarie Boulevard, H4A 3J1, Montreal, QC, Canada.
Vincenzo ArenaDepartment of Obstetrics and Gynecology, Santo Bambino Hospital, via Torre del Vescovo 4, Catania, Italy.
Manuel ArenaDepartment of Surgical Sciences, Organ Transplantation and Advances Technologies, University of Catania, via Santa Sofia 84, Catania, Italy.
Goffredo Orazio ArenaCancer Research Program, McGill University Health Centre-Research Institute, 1001 Decarie Boulevard, Montreal, H4A 3J1, QC, Canada. goffredo.arena@mcgill.ca.
McGill University Health Centre · CABambino Gesù Children's Hospital · ITMcGill University · CAUniversity of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt was reported that metastases might occur via transfer of biologically active blood circulating molecules from the primary tumor to distant organs rather than only migration of cancer cells. We showed in an earlier study that exposure of immortalized human embryonic kidney cells (HEK 293) to cancer patient sera, induce their transformation into undifferentiated cancers due to a horizontal transfer of malignant traits. In the present work, we tested the hypothesis that even other human cells as long as they are deficient for a single oncosuppressor gene might undergo malignant transformation when exposed to human cancer serum.

methodsWe used the CRISPR/Cas9 system to establish a stable BRCA1 knockout (KO) in human fibroblasts. The BRCA1-KO fibroblasts were exposed to cancer patients' sera or healthy patients' sera for 2 weeks. Treated cells were analyzed for cell proliferation and transformation to study their susceptibility to the oncogenic potential of cancer patients' sera and to determine the possible mechanisms underlying their hypothesized transformation.

resultsBRCA1-KO fibroblasts treated with cancer patients' sera displayed higher proliferation and underwent malignant transformation as opposed to wild type control fibroblasts, which were not affected by exposure to cancer patients' sera. The malignant transformation was not seen when BRCA1-KO fibroblasts were treated with healthy human sera. Histological analysis of tumors generated by BRCA1-KO fibroblasts showed that they were carcinomas with phenotypical characteristics related to the cancers of the blood donor patients. Interestingly, BRCA1-KO fibroblasts were significantly more prone to internalize serum-derived exosomes, when compared to wild type fibroblasts. This suggests that oncosuppressor genes might protect the integrity of the cell genome also by blocking integration of cancer-derived exosomes.

conclusionThese data support the hypothesis that any human cells carrying a single oncosuppressor mutation is capable of integrating cancer factors carried in the blood and undergo complete malignant transformation. Oncosuppressor genes might protect the cell genome by impeding the integration inside the cells of these mutating factors.

Indexed as

AdultAgedAnimalsBRCA1 ProteinCell ProliferationCell Transformation, NeoplasticCulture Media, ConditionedFibroblastsGene Knockout TechniquesHEK293 CellsHumansMiceMiddle AgedNeoplasmsNeoplasm TransplantationSerumBRCA1 ProteinBRCA1 protein, humanCulture Media, ConditionedBRCA1ExosomesFibroblastsGenometastasisMetastasisTransformationTumor suppressor genes

Identifiers

PMID27179759
PMCPMC4868000
OpenAlexW2387193491

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.