Evidence map›Paper›PMID 31268155›Full record

ArticleInternational journal of oncology2019

Prognostic significance of VHL, HIF1A, HIF2A, VEGFA and p53 expression in patients with clear‑cell renal cell carcinoma treated with sunitinib as first‑line treatment.

Piotr M Wierzbicki, Jakub Klacz, Anna Kotulak-Chrzaszcz, Agata Wronska, Marcin Stanislawowski, Agnieszka Rybarczyk, Aleksandra Ludziejewska, Zbigniew Kmiec, Marcin Matuszewski

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 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

9 authors at 2 institutions in 1 country.

Piotr M WierzbickiDepartment of Histology, Faculty of Medicine, Medical University of Gdansk, 80211 Gdansk, Poland.
Jakub KlaczDepartment of Urology, Faculty of Medicine, Medical University of Gdansk, 80402 Gdansk, Poland.
Anna Kotulak-ChrzaszczDepartment of Histology, Faculty of Medicine, Medical University of Gdansk, 80211 Gdansk, Poland.
Agata WronskaDepartment of Histology, Faculty of Medicine, Medical University of Gdansk, 80211 Gdansk, Poland.
Marcin StanislawowskiDepartment of Histology, Faculty of Medicine, Medical University of Gdansk, 80211 Gdansk, Poland.
Agnieszka RybarczykDepartment of Histology, Faculty of Medicine, Medical University of Gdansk, 80211 Gdansk, Poland.
Aleksandra LudziejewskaDepartment of Laboratory Diagnostics, Medical University of Poznan, 61701 Poznan, Poland.
Zbigniew KmiecDepartment of Histology, Faculty of Medicine, Medical University of Gdansk, 80211 Gdansk, Poland.
Marcin MatuszewskiDepartment of Urology, Faculty of Medicine, Medical University of Gdansk, 80402 Gdansk, Poland.
Gdańsk Medical University · PLPoznan University of Medical Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC) is the most common subtype of renal cell cancer, characterized by the highest mortality rate among other RCC subtypes due to the occurrence of metastasis and drug resistance following surgery. The Von Hippel‑Lindau tumor suppressor (VHL)‑hypoxia‑inducible factor 1 subunit α (HIF1A)/hypoxia‑inducible factor 2α (HIF2A)‑vascular endothelial growth factor A (VEGFA) protein axis is involved in the development and progression of ccRCC, whereas sunitinib, a tyrosine kinase inhibitor, blocks the binding of VEGFA to its receptor. The aim of the present study was to examine the possible association of the gene expression of VHL, HIF1A, HIF2A, VEGFA and tumor protein P53 (P53) in cancer tissue with the outcome of ccRCC patients who were treated with sunitinib as first‑line therapy following nephrectomy. A total of 36 ccRCC patients were enrolled, 11 of whom were administered sunitinib post‑operatively. Tumor and control samples were collected, and mRNA and protein levels were assessed by reverse transcription‑quantitative polymerase chain reaction and western blot analysis, respectively. High mRNA and protein expression levels of HIF2A and VEGFA were found to be associated with shorter overall survival (OS) and progression‑free survival (PFS) rates, as well as with unfavorable risk factors of cancer recurrence and mortality. Resistance to sunitinib was also observed; the OS and PFS rates were shorter (median OS and PFS: 12 and 6 months, respectively, vs. undetermined). Sunitinib resistance was associated with high HIF2A and VEGFA protein levels (b=0.57 and b=0.69 for OS and PFS, respectively; P<0.001). Taken together, the findings of this study suggest that the protein levels of HIF2A and VEGFA in tumor tissue may serve as independent prognostic factors in ccRCC. ccRCC patients with increased intratumoral HIF2A and VEGFA protein levels, and unaltered VHL protein levels, are not likely to benefit from sunitinib treatment following nephrectomy; however, this hypothesis requires verification by large‑scale replication studies.

Indexed as

AdultAgedAged, 80 and overBasic Helix-Loop-Helix ProteinsBiomarkers, TumorCarcinoma, Renal CellEndothelial PAS Domain-Containing Protein 1FemaleFollow-Up StudiesGene Expression Regulation, NeoplasticHumansHypoxia-Inducible Factor 1, alpha SubunitKidney NeoplasmsMaleMiddle AgedPrognosisBasic Helix-Loop-Helix ProteinsBiomarkers, TumorEndothelial PAS Domain-Containing Protein 1HIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitProtein Kinase InhibitorsSunitinibTP53 protein, humanTumor Suppressor Protein p53Vascular Endothelial Growth Factor AVEGFA protein, humanVHL protein, humanVon Hippel-Lindau Tumor Suppressor Protein

Identifiers

PMID31268155
PMCPMC6615924
OpenAlexW2954662313

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.