Evidence map›Paper›PMID 27473057›Full record

ArticleBMC cancer2016

Heat shock protein 70-2 (HSP70-2) is a novel therapeutic target for colorectal cancer and is associated with tumor growth.

Nirmala Jagadish, Deepak Parashar, Namita Gupta, Sumit Agarwal, Vaishali Suri, Rajive Kumar, Vitusha Suri, Trilok Chand Sadasukhi, Anju Gupta, Abdul S Ansari and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.7field-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

36 citing papers in PubMed, 59 citations in OpenAlex.

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  11. Heat Shock Proteins and HSF1 in Cancer.Frontiers in oncology · 2022
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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

12 authors at 5 institutions in 1 country.

Nirmala JagadishCancer Microarray, Genes and Proteins Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi, 110 067, India.
Deepak ParasharCancer Microarray, Genes and Proteins Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi, 110 067, India.
Namita GuptaCancer Microarray, Genes and Proteins Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi, 110 067, India.
Sumit AgarwalCancer Microarray, Genes and Proteins Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi, 110 067, India.
Vaishali SuriDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Rajive KumarInstitute of Rotary Cancer Hospital, All India Institute of Medical Sciences, New Delhi, India.
Vitusha SuriDepartment of Urology, Mahatma Gandhi Medical College and Hospital, Rajasthan, 302022, India.
Trilok Chand SadasukhiDepartment of Urology, Mahatma Gandhi Medical College and Hospital, Rajasthan, 302022, India.
Anju GuptaDepartment of Pathology, NMC Imaging and Diagnostic Centre, Vidyasagar Institute of Mental Health and Neuro-Sciences, New Delhi, 110065, India.
Abdul S AnsariCentre for Advanced Studies, Department of Zoology, University of Rajasthan, Jaipur, 302 004, India.
Nirmal Kumar LohiyaCentre for Advanced Studies, Department of Zoology, University of Rajasthan, Jaipur, 302 004, India.
Anil SuriCancer Microarray, Genes and Proteins Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi, 110 067, India. anil@nii.res.in.
National Institute of Immunology · INAll India Institute of Medical Sciences · INGandhi Medical College & Hospital · INUniversity of Rajasthan · INInstitute of Mental Health · IN

Funding

Cancer Research UK
6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) is the third leading cause of cancer related deaths worldwide both in men and women. Our recent studies have indicated an association of heat shock protein 70-2 (HSP70-2) with bladder urothelial carcinoma. In the present study, we investigated the association of HSP70-2 with various malignant properties of colorectal cancer cells and clinic-pathological features of CRC in clinical specimens.

methodsHSP70-2 mRNA and protein was investigated expression by RT-PCR, immunohistochemistry, immunofluorescence, flow cytometry and Western blotting in CRC clinical specimens and COLO205 and HCT116 cell lines. Plasmid-based gene silencing approach was employed to study the association of HSP70-2 with various malignant properties of COLO205 and HCT116 cells in in vitro and with tumor progression in in vivo COLO205 human xenograft mice model.

resultsHSP70-2 expression was detected in 78 % of CRC patients irrespective of various stages and grades by RT-PCR and IHC. Our analysis further revealed that HSP70-2 expression was detected in both COLO205 and HCT116 cell lines. Ablation of HSP70-2 expression resulted in reduced cellular growth, colony forming ability, migratory and invasive ability of CRC cells. In addition, ablation of HSP70-2 expression showed significant reduction in tumor growth in COLO205 human xenograft in in vivo mouse model.

conclusionCollectively, our results indicate that HSP70-2 is associated with CRC clinical specimens. In addition, down regulation of HSP70-2 expression reduces cellular proliferation and tumor growth indicating that HSP70-2 may be a potential therapeutic target for CRC treatment.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBlotting, WesternCell Line, TumorCell MovementCell ProliferationCell SurvivalColorectal NeoplasmsHCT116 CellsHSP70 Heat-Shock ProteinsHumansImmunohistochemistryMice, SCIDReverse Transcriptase Polymerase Chain ReactionRNA InterferenceRNAi TherapeuticsHSP70 Heat-Shock ProteinsHSPA1B protein, humanCancer testis antigenGene silencingHSP70-2Therapeutic target

Identifiers

PMID27473057
PMCPMC4966739
OpenAlexW2502404460

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LicenceCC BY
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Registered trials

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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.