Evidence map›Paper›PMID 29050201›Full record

ArticleOncotarget2017

HTLV-1 viral oncogene HBZ induces osteolytic bone disease in transgenic mice.

Alison K Esser, Daniel A Rauch, Jingyu Xiang, John C Harding, Nicole A Kohart, Michael H Ross, Xinming Su, Kevin Wu, Devra Huey, Yalin Xu and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Mouse Models for HTLV-1 Infection and Adult T Cell Leukemia.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. When Viruses Cross Developmental Pathways.Frontiers in cell and developmental biology · 2021
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
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

16 authors at 2 institutions in 1 country.

Alison K EsserDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Daniel A RauchDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Jingyu XiangDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
John C HardingDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Nicole A KohartDepartment of Veterinary Biosciences, School of Veterinary Medicine, The Ohio State University, Columbus, OH, USA.
Michael H RossDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Xinming SuDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Kevin WuDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Devra HueyDepartment of Veterinary Biosciences, School of Veterinary Medicine, The Ohio State University, Columbus, OH, USA.
Yalin XuDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Kiran VijDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Patrick L GreenDepartment of Veterinary Biosciences, School of Veterinary Medicine, The Ohio State University, Columbus, OH, USA.
Thomas J RosolDepartment of Veterinary Biosciences, School of Veterinary Medicine, The Ohio State University, Columbus, OH, USA.
Stefan NiewieskDepartment of Veterinary Biosciences, School of Veterinary Medicine, The Ohio State University, Columbus, OH, USA.
Lee RatnerDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Katherine N WeilbaecherDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Washington University in St. Louis · USThe Ohio State University · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Daniel G. Stover · 1985 to 2026
$132.3M
Role of Inflammation in Tax-mediated TumorigenesisP01CA100730 · NCI · WASHINGTON UNIVERSITY · PI Lee Ratner · 2003 to 2026
$44.8M
TRAINING PROGRAM IN CELLULAR AND MOLECULAR BIOLOGYT32GM007067 · NIGMS · WASHINGTON UNIVERSITY · PI TRUE-KROB, HEATHER L · 1985 to 2020
$20.4M
The Role of the Osteoblast Secretome in Bone FormationP30AR057235 · NIAMS · WASHINGTON UNIVERSITY · PI SWARNKAR, GAURAV · 2009 to 2018
$5.7M
MOLECULAR ONCOLOGY TRAINING GRANTT32CA113275 · NCI · WASHINGTON UNIVERSITY · PI Matthew J Walter · 2006 to 2026
$5.7M
Skeletal Disorders Training ProgramT32AR060719 · NIAMS · WASHINGTON UNIVERSITY · PI Roberto Civitelli · 2011 to 2026
$4.6M
PROLIFERATIVE EFFECTS OF HTLV1R01CA063417 · NCI · WASHINGTON UNIVERSITY · PI RATNER, LEE · 1995 to 2017
$3.7M
NEXT GENERATION APPROACHES TO BREAST CANCER USING IMAGE GUIDED DRUG DELIVERYR01CA154737 · NCI · WASHINGTON UNIVERSITY · PI LANZA, GREGORY M, PAN, DIPANJAN · 2011 to 2015
$2.4M
Mouse Pathobiology: Models of Human DiseaseT32OD010429 · OD · OHIO STATE UNIVERSITY · PI NIEWIESK, STEFAN, OGLESBEE, MICHAEL J · 2012 to 2017
$1.3M
WHOLE SLIDE IMAGING SYSTEM FOR TRANSLATIONAL NEUROSCIENCES10RR027552 · NCRR · WASHINGTON UNIVERSITY · PI LEE, JIN-MOO · 2010 to 2010
$275k
Integrin AVB3 Targeted Nanoparticles as a Novel Therapy of Bone MetastasesF32CA189671 · NCI · WASHINGTON UNIVERSITY · PI ESSER, ALISON · 2014 to 2015
$109k
NCI NIH HHS F32 CA189671NCI NIH HHS P01 CA100730NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA063417NCI NIH HHS R01 CA154737NCI NIH HHS T32 CA113275NCRR NIH HHS S10 RR027552NIAMS NIH HHS P30 AR057235NIAMS NIH HHS T32 AR060719NIGMS NIH HHS T32 GM007067NIH HHS T32 OD010429
6 · The paper itself

Abstract

Adult T-cell leukemia/lymphoma (ATL) is an aggressive T cell malignancy that occurs in HTLV-1 infected patients. Most ATL patients develop osteolytic lesions and hypercalcemia of malignancy, causing severe skeletal related complications and reduced overall survival. The HTLV-1 virus encodes 2 viral oncogenes, Tax and HBZ. Tax, a transcriptional activator, is critical to ATL development, and has been implicated in pathologic osteolysis. HBZ, HTLV-1 basic leucine zipper transcription factor, promotes tumor cell proliferation and disrupts Wnt pathway modulators; however, its role in ATL induced osteolytic bone loss is unknown. To determine if HBZ is sufficient for the development of bone loss, we established a transgenic Granzyme B HBZ (Gzmb-HBZ) mouse model. Lymphoproliferative disease including tumors, enlarged spleens and/or abnormal white cell counts developed in two-thirds of Gzmb-HBZ mice at 18 months. HBZ positive cells were detected in tumors, spleen and bone marrow. Importantly, pathologic bone loss and hypercalcemia were present at 18 months. Bone-acting factors were present in serum and RANKL, PTHrP and DKK1, key mediators of hypercalcemia and bone loss, were upregulated in Gzmb-HBZ T cells. These data demonstrate that Gzmb-HBZ mice model ATL bone disease and express factors that are current therapeutic targets for metastatic and bone resident tumors.

Indexed as

ATLboneHBZHTLV-1leukemia

Identifiers

PMID29050201
PMCPMC5642476
OpenAlexW2746493964

What Socratic 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 Socratic graph.