Evidence map›Paper›PMID 27637088›Full record

ArticleOncotarget2016

Evolution of malignant plasmacytoma cell lines from K14E7 Fancd2-/- mouse long-term bone marrow cultures.

Xichen Zhang, Wen Hou, Michael W Epperly, Lora Rigatti, Hong Wang, Darcy Franicola, Aranee Sivanathan, Joel S Greenberger

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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

8 authors at 2 institutions in 1 country.

Xichen ZhangDepartment of Radiation Oncology, University of Pittsburgh Cancer Institute, Pittsburgh, 15232 PA, USA.
Wen HouDepartment of Radiation Oncology, University of Pittsburgh Cancer Institute, Pittsburgh, 15232 PA, USA.
Michael W EpperlyDepartment of Radiation Oncology, University of Pittsburgh Cancer Institute, Pittsburgh, 15232 PA, USA.
Lora RigattiDivision of Laboratory Animal Resources, University of Pittsburgh, Pittsburgh, 15260 PA, USA.
Hong WangDepartment of Radiation Oncology, University of Pittsburgh Cancer Institute, Pittsburgh, 15232 PA, USA.
Darcy FranicolaDepartment of Radiation Oncology, University of Pittsburgh Cancer Institute, Pittsburgh, 15232 PA, USA.
Aranee SivanathanDepartment of Radiation Oncology, University of Pittsburgh Cancer Institute, Pittsburgh, 15232 PA, USA.
Joel S GreenbergerDepartment of Radiation Oncology, University of Pittsburgh Cancer Institute, Pittsburgh, 15232 PA, USA.
UPMC Hillman Cancer Center · USUniversity of Pittsburgh · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHN C. BYRD · 1988 to 2026
$158.0M
NCI NIH HHS P30 CA047904
6 · The paper itself

Abstract

We tested the effect of expression of the Human Papilloma Virus (HPV E7) oncogene on hematopoiesis in long-term bone marrow cultures (LTBMCs) derived from K14E7 (FVB) Fancd2-/- (129/Sv), K14E7 Fancd2+/+, Fancd2-/-, and control (FVB X 129/Sv) Fl mice. K14E7 Fancd2-/- and Fancd2-/- LTBMCs showed decreased duration of production of total nonadherent hematopoietic cells and progenitors forming day 7 and day 14 multilineage CFU-GEMM colonies in secondary cultures (7 wks and 8 wks respectively) compared to cultures from K14E7 Fancd2+/+ (17 wks) or control mice (18 wks) p < 0.0001. Marrow stromal cell lines derived from both K14E7 Fancd2-/- and Fancd2-/- cultures were radiosensitive, as were IL-3 dependent hematopoietic progenitor cell lines derived from K14E7 Fancd2-/- cultures. In contrast, Fancd2-/- mouse hematopoietic progenitor cell lines and fresh marrow were radioresistant. K14E7 Fancd2-/- mouse freshly explanted bone marrow expressed no detectable K14 or E7; however, LTBMCs produced K14 positive factor-independent (FI) clonal malignant plasmacytoma forming cell lines in which E7 was detected in the nucleus with p53 and Rb. Transfection of an E6/E7 plasmid into Fancd2-/-, but not control Fancd2+/+ IL-3 dependent hematopoietic progenitor cell lines, increased cloning efficiency, cell growth, and induced malignant cell lines. Therefore, the altered radiobiology of hematopoietic progenitor cells and malignant transformation in vitro by K14E7 expression in cells of the Fancd2-/- genotype suggests a potential role of HPV in hematopoietic malignancies in FA patients.

Indexed as

AnimalsBone Marrow CellsCell Line, TumorCells, CulturedCell SurvivalFanconi AnemiaFanconi Anemia Complementation Group D2 ProteinHematopoiesisHematopoietic Stem CellsHumansKeratin-14Mice, 129 StrainMice, Inbred C57BLMice, KnockoutPapillomavirus E7 ProteinsPlasmacytomaFanconi Anemia Complementation Group D2 ProteinKeratin-14Papillomavirus E7 ProteinsE7Fancd2−/− miceFanconi anemiaHPV oncogenehuman papillomavirus

Identifiers

PMID27637088
PMCPMC5356567
OpenAlexW2520438979

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.