Evidence map›Paper›PMID 37927802›Full record

ReviewCancer diagnosis & prognosis

An Overview of Renal Cell Carcinoma Hallmarks, Drug Resistance, and Adjuvant Therapies.

Josiele DA Silva Prade, Ruan Soares DE Souza, Camila Medianeira DA Silva D'Αvila, Thayline Correia DA Silva, Isadora Cassel Livinalli, Ana Clara Zanini Bertoncelli, Fernanda Krapf Saccol, Tallys DE Oliveira Mendes, Larissa Gindri Wenning, Theodoro DA Rosa Salles and 2 more

Abstract readReview
In one paragraph

Review in Cancer diagnosis & prognosis. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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.

Josiele DA Silva PradePost-graduate Program in Health and Life Sciences, Franciscan University, Santa Maria, RS, Brazil.
Ruan Soares DE SouzaMedicine Graduate Course, Franciscan University, Santa Maria, RS, Brazil.
Camila Medianeira DA Silva D'ΑvilaBiomedicine Graduate Course, Franciscan University, Santa Maria, RS, Brazil.
Thayline Correia DA SilvaBiomedicine Graduate Course, Franciscan University, Santa Maria, RS, Brazil.
Isadora Cassel LivinalliBiomedicine Graduate Course, Franciscan University, Santa Maria, RS, Brazil.
Ana Clara Zanini BertoncelliBiomedicine Graduate Course, Franciscan University, Santa Maria, RS, Brazil.
Fernanda Krapf SaccolBiomedicine Graduate Course, Franciscan University, Santa Maria, RS, Brazil.
Tallys DE Oliveira MendesBiomedicine Graduate Course, Franciscan University, Santa Maria, RS, Brazil.
Larissa Gindri WenningPharmacy Graduate Course, Franciscan University, Santa Maria, RS, Brazil.
Theodoro DA Rosa SallesLaboratory of Nanostructured Magnetic Materials - LaMMaN, Franciscan University, Santa Maria, RS, Brazil.
Cristiano Rodrigo Bohn RhodenLaboratory of Nanostructured Magnetic Materials - LaMMaN, Franciscan University, Santa Maria, RS, Brazil.
Francine Carla CadonaPost-graduate Program in Health and Life Sciences, Franciscan University, Santa Maria, RS, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal neoplasms are highlighted as one of the 10 most common types of cancer. Renal cell carcinoma (RCC) is the most common type of renal cancer, considered the seventh most common type of cancer in the Western world. The most frequently altered genes described as altered are VHL, PBRM1, SETD2, KDM5C, PTEN, BAP1, mTOR, TP53, TCEB1 (ELOC), SMARCA4, ARID1A, and PIK3CA. RCC therapies can be classified in three groups: monoclonal antibodies, tyrosine kinase inhibitors, and mTOR inhibitors. Besides, there are targeted agents to treat RCC. However, frequently patients present side effects and resistance. Even though many multidrug resistance mechanisms already have been reported to RCC, studies focused on revealing new biomarkers as well as more effective antitumor therapies with no or low side effects are very important. Some studies reported that natural products, such as honey, epigallocatechin-3-gallate (EGCG), curcumin, resveratrol, and englerin A showed antitumor activity against RCC. Moreover, nanoscience is another strategy to improve RCC treatment and reduce the side effects due to the improvement in pharmacokinetics and reduction of toxicities of chemotherapies. Taking this into account, we conducted a systemic review of recent research findings on RCC hallmarks, drug resistance, and adjuvant therapies. In conclusion, a range of studies reported that RCC is characterized by high incidence and increased mortality rates because of the development of resistance to standard therapies. Given the importance of improving RCC treatment and reducing adverse effects, nanoscience and natural products can be included in therapeutic strategies.

Indexed as

anticancer treatmentsnanosciencenatural productsRenal neoplasmreview

Identifiers

PMID37927802
PMCPMC10619564

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.