Evidence map›Paper›PMID 31963898›Full record

ArticleCancers2020

Sterol O-Acyl Transferase 1 as a Prognostic Marker of Adrenocortical Carcinoma.

Amanda Meneses Ferreira Lacombe, Iberê Cauduro Soares, Beatriz Marinho de Paula Mariani, Mirian Yumie Nishi, João Evangelista Bezerra-Neto, Helaine da Silva Charchar, Vania Balderrama Brondani, Fabio Tanno, Victor Srougi, José Luiz Chambo and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. [p53-SOAT1 Axis: A Novel Target for Tumor Lipid Metabolism and Therapy].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. The Challenging Pharmacokinetics of Mitotane: An Old Drug in Need of New Packaging.European journal of drug metabolism and pharmacokinetics · 2021
    Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Low Protein Expression of bothInternational journal of molecular sciences · 2021
    Article
  18. Article
  19. Review
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

18 authors at 3 institutions in 2 countries.

Amanda Meneses Ferreira LacombeUnidade de Suprarrenal, Laboratório de Hormônios e Genética Molecular LIM/42, Serviço de Endocrinologia e Metabologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Enéas de Carvalho Aguiar, 155, São Paulo, SP 05403-900, Brazil.ORCID 0000-0001-6383-4668
Iberê Cauduro SoaresServiço de Anatomia Patológica, Instituto do Câncer do Estado de São Paulo (ICESP), Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Arnaldo, 251, São Paulo, SP 01246-000, Brazil.
Beatriz Marinho de Paula MarianiUnidade de Suprarrenal, Laboratório de Hormônios e Genética Molecular LIM/42, Serviço de Endocrinologia e Metabologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Enéas de Carvalho Aguiar, 155, São Paulo, SP 05403-900, Brazil.
Mirian Yumie NishiUnidade de Suprarrenal, Laboratório de Hormônios e Genética Molecular LIM/42, Serviço de Endocrinologia e Metabologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Enéas de Carvalho Aguiar, 155, São Paulo, SP 05403-900, Brazil.
João Evangelista Bezerra-NetoServiço de Oncologia Clínica, Instituto do Câncer do Estado de São Paulo (ICESP), Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Arnaldo, 251, São Paulo, SP 01246-000, Brazil.ORCID 0000-0002-6069-8426
Helaine da Silva CharcharUnidade de Suprarrenal, Laboratório de Hormônios e Genética Molecular LIM/42, Serviço de Endocrinologia e Metabologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Enéas de Carvalho Aguiar, 155, São Paulo, SP 05403-900, Brazil.
Vania Balderrama BrondaniUnidade de Suprarrenal, Laboratório de Hormônios e Genética Molecular LIM/42, Serviço de Endocrinologia e Metabologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Enéas de Carvalho Aguiar, 155, São Paulo, SP 05403-900, Brazil.
Fabio TannoServiço de Urologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Av. Dr Enéas de Carvalho Aguiar, 255, São Paulo, SP 05403-000, Brazil.
Victor SrougiServiço de Urologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Av. Dr Enéas de Carvalho Aguiar, 255, São Paulo, SP 05403-000, Brazil.
José Luiz ChamboServiço de Urologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Av. Dr Enéas de Carvalho Aguiar, 255, São Paulo, SP 05403-000, Brazil.
Ricardo Miguel Costa de FreitasServiço de Radiologia, Instituto do Câncer do Estado de São Paulo (ICESP), Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Arnaldo, 251, São Paulo, SP 01246-000, Brazil.
Berenice Bilharinho MendoncaUnidade de Suprarrenal, Laboratório de Hormônios e Genética Molecular LIM/42, Serviço de Endocrinologia e Metabologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Enéas de Carvalho Aguiar, 155, São Paulo, SP 05403-900, Brazil.
Ana O HoffServiço de Endocrinologia, Instituto do Câncer do Estado de São Paulo (ICESP), Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Arnaldo, 251, São Paulo, SP 01246-000, Brazil.
Madson Q AlmeidaUnidade de Suprarrenal, Laboratório de Hormônios e Genética Molecular LIM/42, Serviço de Endocrinologia e Metabologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Enéas de Carvalho Aguiar, 155, São Paulo, SP 05403-900, Brazil.
Isabel WeigandDepartamento de Medicina Interna, Unidade de Endocrinologia e Diabetes, Hospital da Universidade de Würzburg, Josef-Schneider-Straße, 97080 Würzburg, Germany.
Matthias KroissDepartamento de Medicina Interna, Unidade de Endocrinologia e Diabetes, Hospital da Universidade de Würzburg, Josef-Schneider-Straße, 97080 Würzburg, Germany.
Maria Claudia Nogueira ZerbiniDepartamento de Anatomia Patológica, Faculdade de Medicina da Universidade de São Paulo, Av. Dr Arnaldo, 455, São Paulo, SP 01246-903, Brazil.
Maria Candida Barisson Villares FragosoUnidade de Suprarrenal, Laboratório de Hormônios e Genética Molecular LIM/42, Serviço de Endocrinologia e Metabologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Enéas de Carvalho Aguiar, 155, São Paulo, SP 05403-900, Brazil.
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRUniversidade de São Paulo · BRUniversitätsklinikum Würzburg · DE

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 2018/140242Fundação de Amparo à Pesquisa do Estado de São Paulo 2017/26345-5
6 · The paper itself

Abstract

Adrenocortical carcinoma (ACC) is a rare endocrine malignancy with an unfavorable prognosis. Despite the poor prognosis in the majority of patients, no improvements in treatment strategies have been achieved. Therefore, the discovery of new prognostic biomarkers is of enormous interest. Sterol-O-acyl transferase 1 (SOAT1) is involved in cholesterol esterification and lipid droplet formation. Recently, it was demonstrated that SOAT1 inhibition leads to impaired steroidogenesis and cell viability in ACC. To date, no studies have addressed the impact of SOAT1 expression on ACC prognosis and clinical outcomes. We evaluated SOAT1 expression by quantitative real-time polymerase chain reaction and immunohistochemistry in a tissue microarray of 112 ACCs (Weiss score ≥ 3) from adults treated in a single tertiary center in Brazil. Two independent pathologists evaluated the immunohistochemistry results through a semiquantitative approach (0-4). We aimed to evaluate the correlation between SOAT1 expression and clinical, biochemical and anatomopathological parameters, recurrence-free survival (RFS), progression-free survival (PFS), and overall survival (OS). SOAT1 protein expression was heterogeneous in this cohort, 37.5% of the ACCs demonstrated a strong SOAT1 protein expression (score > 2), while 62.5% demonstrated a weak or absent protein expression (score ≤ 2). Strong SOAT1 protein expression correlated with features of high aggressiveness in ACC, such as excessive tumor cortisol secretion (

Indexed as

adrenocortical carcinomaprognostic factorsSOAT1target therapies

Identifiers

PMID31963898
PMCPMC7016635
OpenAlexW2998964116

What OpenQuestion holds

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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.