Evidence map›Paper›PMID 29422892›Full record

ArticleFrontiers in immunology2017

Cathepsin G Is Expressed by Acute Lymphoblastic Leukemia and Is a Potential Immunotherapeutic Target.

Maliha Khan, Selena Carmona, Pariya Sukhumalchandra, Jason Roszik, Anne Philips, Alexander A Perakis, Celine Kerros, Mao Zhang, Na Qiao, Lisa S St John and 10 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 26 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

20 authors at 1 institution in 1 country.

Maliha KhanDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, United States.
Selena CarmonaDepartment of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, TX, United States.
Pariya SukhumalchandraDepartment of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, TX, United States.
Jason RoszikDepartment of Melanoma Medical Oncology, MD Anderson Cancer Center, Houston, TX, United States.
Anne PhilipsSurgical Oncology, MD Anderson Cancer Center, Houston, TX, United States.
Alexander A PerakisDepartment of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, TX, United States.
Celine KerrosDepartment of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, TX, United States.
Mao ZhangDepartment of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, TX, United States.
Na QiaoDepartment of Genomic Medicine, MD Anderson Cancer Center, Houston, TX, United States.
Lisa S St JohnDepartment of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, TX, United States.
Madhushree ZopeDepartment of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, TX, United States.
Jonathan GoldbergSurgical Oncology, MD Anderson Cancer Center, Houston, TX, United States.
Mariam QazilbashDepartment of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, TX, United States.
Haroon JakherDepartment of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, TX, United States.
Karen Clise-DwyerDepartment of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, TX, United States.
Yihua QiuDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, United States.
Elizabeth A MittendorfSurgical Oncology, MD Anderson Cancer Center, Houston, TX, United States.
Jeffrey J MolldremDepartment of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, TX, United States.
Steven M KornblauDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, United States.
Gheath AlatrashDepartment of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, TX, United States.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
University of Texas M.D. Anderson Cancer SPORE-LeukemiaP50CA100632 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KONOPLEVA, MARINA Y · 2003 to 2023
$43.7M
NCI NIH HHS P50 CA100632
6 · The paper itself

Abstract

Cathepsin G (CG) is a myeloid azurophil granule protease that is highly expressed by acute myeloid leukemia (AML) blasts and leukemia stem cells. We previously identified CG1 (FLLPTGAEA), a human leukocyte antigen-A2-restricted nonameric peptide derived from CG, as an immunogenic target in AML. In this report, we aimed to assess the level of CG expression in acute lymphoid leukemia (ALL) and its potential as an immunotherapeutic target in ALL. Using RT-PCR and western blots, we identified CG mRNA and protein, respectively, in B-ALL patient samples and cell lines. We also examined CG expression in a large cohort of 130 patients with ALL

Indexed as

acute lymphoblastic leukemiaantigenscathespin Gcross-presentationimmunotherapynonameric peptideserine proteasestargeted therapy

Identifiers

PMID29422892
PMCPMC5790053
OpenAlexW2788480653

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.