Carolina Pereira de Souza Melo

Dr. Carolina Pereira de Souza Melo


Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2013 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
LSLívia B. Salum
Lívia B. Salum
WAWanessa Fernanda Altei
Wanessa Fernanda Altei
LCLouise D. Chiaradia
Louise D. Chiaradia
MCMarlon N.S. Cordeiro
Marlon N.S. Cordeiro
RCRafael R. Canevarolo
Rafael R. Canevarolo
AVAndreas Vogt
Andreas Vogt

1 May 2015 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
LSLívia B. Salum
Lívia B. Salum
AMAlessandra Mascarello
Alessandra Mascarello
RCRafael R. Canevarolo
Rafael R. Canevarolo
WAWanessa Fernanda Altei
Wanessa Fernanda Altei
ALAngelo B.A. Laranjeira
Angelo B.A. Laranjeira
RNRicardo J. Nunes
Ricardo J. Nunes

1 February 2015 in Leukemia Research
Verified
Journal Article
Closed access
CMCarolina Pereira de Souza Melo
Carolina Pereira de Souza Melo
CCCatharina Brant Campos
Catharina Brant Campos
ÁDÁlvaro Pimenta Dutra
Álvaro Pimenta Dutra
JNJoaquim Caetano Aguirre Neto
Joaquim Caetano Aguirre Neto
AFAlexandre José Silva Fenelon
Alexandre José Silva Fenelon
JAJuliana Godoy Assumpcão
Juliana Godoy Assumpcão

23 July 2015 in British Journal of Haematology
Verified
Journal Article
Open access
PDF file
CMCarolina Pereira de Souza Melo
Carolina Pereira de Souza Melo
CCCatharina B. Campos
Catharina B. Campos
JRJuliana de Oliveira Rodrigues
Juliana de Oliveira Rodrigues
JAJoaquim C. Aguirre‐Neto
Joaquim C. Aguirre‐Neto
ÂAÂngelo Atalla
Ângelo Atalla
JAJuliana G. Assumpção
Juliana G. Assumpção
The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.

1 April 2025 in Non-coding RNA Research
Verified
Journal Article
Open access
BDBruna Custódio Dias Duarte
Bruna Custódio Dias Duarte
FQFábio Ribeiro Queiroz
Fábio Ribeiro Queiroz
ÁCÁlvaro Percínio Costa
Álvaro Percínio Costa
ANAngelo Borges de Melo Neto
Angelo Borges de Melo Neto
CMCarolina Pereira de Souza Melo
Carolina Pereira de Souza Melo
AFAgnaldo Lopes da Silva Filho
Agnaldo Lopes da Silva Filho
Cervical cancer (CC) is a global public health concern, primarily caused by persistent infection with oncogenic types of human papillomavirus (HPV). The World Health Organization (WHO) has established a plan to eliminate CC as a public health issue by the year 2100. However, the implementation of the HPV vaccine is impeded by vaccine restrictions and misinformation despite its demonstrated effectiveness. The CC treatment is influenced by the disease stage, with an unfavorable prognosis for those in advanced stages. This study aimed to investigate the potential of long non-coding RNAs (lncRNAs) in CC by identifying and characterizing related lncRNAs, elucidating their regulatory mechanisms and molecular interactions, and analyzing their expression patterns in patients with diverse responses to chemoradiotherapy. Non-stem cells from CC were isolated using flow cytometry sorting and used for total RNA extraction. The RNA was used to build libraries that were subsequently sequenced using the Illumina Nextseq 550.417 lncRNAs that showed differentially expressed between CC patients who responded or not to treatment. Further analysis demonstrated that these lncRNAs significantly interact with several molecules, which play crucial roles in CC progression and therapeutic resistance. Statistical analysis correlated the expression profile of these lncRNAs with treatment efficacy. Three lncRNAs, ENSG00000267838, ENSG00000266340, and FRMD6-AS1, were identified with positive expression related to non-response to chemoradiotherapy and worse progression-free survival in CC patients. Specifically, lncRNA ENSG00000267838 has its up-regulation related to non-response and down-regulation to response to chemoradiotherapy treatment.

1 August 2002 in Microscopy and Microanalysis
Verified
Journal Article
Closed access
PDF file
CMCarolina Pereira de Souza Melo
Carolina Pereira de Souza Melo
MAMargareth Spangler Andrade
Margareth Spangler Andrade
BNBernardo Ruegger Almeida Neves
Bernardo Ruegger Almeida Neves
In this work, effective, yet simple, recycling mechanisms for used scanning probe microscopy (SPM) tips were implemented. Comprising a tip profile characterization methodology and specific cleaning procedures, which decontaminate SPM tips whether the contamination nature is known or not, such routes were optimized during numerous tests with brand new, previously used, and already discarded categories of SPM tips. The results show that if the used tip suffered contamination only, but no physical damages, during its scanning lifetime, it becomes readily available for reutilization after the cleansing process, characterizing a recycling route. On the other hand, if the tip went through wear and breakages during its utilization, it still can be decontaminated, but may not be directly reutilized due to its inadequate physical profile. Nevertheless, the methodology developed in this work may yet be applied as part of a more complex recycling route.