Evidence map›Paper›PMID 32815150›Full record

ArticleThe Journal of pathology2020

Features of increased malignancy in eosinophilic clear cell renal cell carcinoma.

Helén Nilsson, David Lindgren, Håkan Axelson, Christian Brueffer, Lao H Saal, Jaana Lundgren, Martin E Johansson

Open access · hybridAbstract read
In one paragraph

Article in The Journal of pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

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  7. Mutated ASXL1 upregulates mTOR expression in renal cell carcinoma with fibromyomatous stroma.Virchows Archiv : an international journal of pathology · 2024
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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

7 authors at 2 institutions in 1 country.

Helén NilssonDepartment of Translational Medicine, Lund University, Malmö, Sweden.
David LindgrenDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Håkan AxelsonDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Christian BruefferDivision of Oncology, Department of Clinical Sciences, Lund University, Lund, Sweden.ORCID 0000-0002-3826-0989
Lao H SaalDivision of Oncology, Department of Clinical Sciences, Lund University, Lund, Sweden.
Jaana LundgrenClinical Pathology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Martin E JohanssonClinical Pathology, Sahlgrenska University Hospital, Gothenburg, Sweden.ORCID 0000-0001-8510-3102
Lund University · SESahlgrenska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC) is the most common form of renal cancer. Due to inactivation of the von Hippel-Lindau tumour suppressor, the hypoxia-inducible transcription factors (HIFs) are constitutively activated in these tumours, resulting in a pseudo-hypoxic phenotype. The HIFs induce the expression of genes involved in angiogenesis and cell survival, but they also reset the cellular metabolism to protect cells from oxygen and nutrient deprivation. ccRCC tumours are highly vascularized and the cytoplasm of the cancer cells is filled with lipid droplets and glycogen, resulting in the histologically distinctive pale (clear) cytoplasm. Intratumoural heterogeneity may occur, and in some tumours, areas with granular, eosinophilic cytoplasm are found. Little is known regarding these traits and how they relate to the coexistent clear cell component, yet eosinophilic ccRCC is associated with higher grade and clinically more aggressive tumours. In this study, we have for the first time performed RNA sequencing comparing histologically verified clear cell and eosinophilic areas from ccRCC tissue, aiming to analyse the characteristics of these cell types. Findings from RNA sequencing were confirmed by immunohistochemical staining of biphasic ccRCC. We found that the eosinophilic phenotype displayed a higher proliferative drive and lower differentiation, and we confirmed a correlation to tumours of higher stage. We further identified mutations of the tumour suppressor p53 (TP53) exclusively in the eosinophilic ccRCC component, where mTORC1 activity was also elevated. Also, eosinophilic areas were less vascularized, yet harboured more abundant infiltrating immune cells. The cytoplasm of clear cell ccRCC cells was filled with lipids but had very low mitochondrial content, while the reverse was found in eosinophilic tissue. We herein suggest possible transcriptional mechanisms behind these phenomena. © 2020 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd. on behalf of The Pathological Society of Great Britain and Ireland.

Indexed as

Gene Expression Regulation, NeoplasticCarcinoma, Renal CellCell ProliferationEosinophiliaHumansKidney NeoplasmsMutationSequence Analysis, RNASignal TransductionTumor Suppressor Protein p53Von Hippel-Lindau Tumor Suppressor ProteinTP53 protein, humanTumor Suppressor Protein p53Von Hippel-Lindau Tumor Suppressor Proteinclear cellelectron microscopyeosinophilicgranularkidney cancermitochondriamTORp53renal cell carcinomavasculatureVHL

Identifiers

PMID32815150
PMCPMC7756750
OpenAlexW3080972274

What OpenQuestion holds

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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.