Evidence map›Paper›PMID 15357873›Full record

ArticleBMC urology2004

Collecting duct carcinoma of the kidney: an immunohistochemical study of 11 cases.

Andrea Vecchione, Tommaso Prayer Galetti, Marina Gardiman, Hideshi Ishii, Enrico Giarnieri, Francesco Pagano, Leonard G Gomella, Carlo M Croce, Raffaele Baffa

Open access · goldAbstract read
In one paragraph

Article in BMC urology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

9 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
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  4. Diffuse leptomeningeal glioneuronal tumors: a new entity?Brain pathology (Zurich, Switzerland) · 2010
    Article
  5. Article
  6. Article
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  9. Collecting duct of Bellini renal carcinoma with psoas muscle recurrence: A case report and review of literature.Canadian Urological Association journal = Journal de l'Association des urologues du Canada
    Article
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 4 institutions in 3 countries.

Andrea VecchioneDepartment of Urology, Kimmel Cancer Center, Thomas Jefferson University, 1025 Walnut Street, Philadelphia, PA, 19107, USA. a_vecchione@mail.jci.tju.edu
Tommaso Prayer Galetti
Marina Gardiman
Hideshi Ishii
Enrico Giarnieri
Francesco Pagano
Leonard G Gomella
Carlo M Croce
Raffaele Baffa
Thomas Jefferson University · USUniversity of Padua · ITAzienda Ospedaliera Sant'Andrea · ITSidney Kimmel Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCollecting duct carcinoma (CDC) is a rare but very aggressive variant of kidney carcinoma that arises from the epithelium of Bellini's ducts, in the distal portion of the nephron. In order to gain an insight into the biology of this tumor we evaluated the expression of five genes involved in the development of renal cancer (FEZ1/LZTS1, FHIT, TP53, P27kip1, and BCL2).

methodsWe studied eleven patients who underwent radical nephrectomy for primary CDC. All patients had an adequate clinical follow-up and none of them received any systemic therapy before surgery. The expression of the five markers for tumor initiation and/or progression were assessed by immunohistochemistry and correlated to the clinicopathological parameters, and survival by univariate analysis.

resultsResults showed that Fez1 protein expression was undetectable or substantially reduced in 7 of the 11 (64%) cases. Fhit protein was absent in three cases (27%). The overexpression of p53 protein was predominantly nuclear and detected in 4 of 11 cases (36%). Immunostaining for p27 was absent in 5 of 11 cases (45.5%). Five of the six remaining cases (90%) showed exclusively cytoplasmic protein expression, where, in the last case, p27 protein was detected in both nucleus and cytoplasm. Bcl2 expression with 100% of the tumor cells positive was observed in 4 of 11 (36%) cases. Statistical analysis showed a statistical trend (P = 0.06) between loss and reduction of Fez1 and presence of lymph node metastases.

conclusionsThese findings suggest that Fez1 may represent not only a molecular diagnostic marker but also a prognostic marker in CDC.

Indexed as

Acid Anhydride HydrolasesAdultAgedAged, 80 and overBis(5'-adenosyl)triphosphataseCarcinoma, DuctalCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor p27FemaleHumansImmunohistochemistryKidney NeoplasmsMaleMiddle AgedNeoplasm ProteinsProto-Oncogene Proteins c-bcl-2Acid Anhydride HydrolasesBis(5'-adenosyl)triphosphataseCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor p27Neoplasm ProteinsProto-Oncogene Proteins c-bcl-2Tumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID15357873
PMCPMC517938
OpenAlexW2140727236

What OpenQuestion holds

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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.