
Our Metabolism Research and Published Papers
FULL PAPERS
Plasma metabolic signatures in epithelial ovarian cancer diagnosis: The application of NextGen Metabolomics in gynecologic oncology.
P D'Amora, IDCG Silva, AJ Nagourney, SS Evans… - 2025
e17593 Background: Epithelial ovarian cancer (EOC) is the most lethal gynecologic malignancy. The lack of reliable diagnostic tests for early detection has led to the majority of EOC patients being diagnosed with advanced stage disease. Despite …
Heading 6
Use of plasma metabolomic profile to predict breast cancer survival: Risk stratification based on tumor nutrient dependencies.
M Salzgeber, P D'Amora, IDCG Silva, LA Belli… - 2025
e12545 Background: Breast cancer is the most common cancer in women. Metabolic reprogramming is a hallmark of the disease. The propensity of cancer cells to exploit exogenous nutrient sources (auxotrophy) may offer insights into breast cancer …
Heading 6
Plasma metabolomic signatures for predicting pancreatic ductal adenocarcinoma survival: The clinical application of targeted mass spectrometry lipidomics.
P D'Amora, IDCG Silva, AJ Nagourney, F Francisco… - 2025
e16409 Background: Pancreatic ductal adenocarcinoma (PDAC) is one the most lethal human cancers with an overall 5-year survival of 12%. Diagnostic and prognostic biomarkers have the potential to improve early detection and the hope for …
Heading 6
PP098. Lipidic fingerprinting in women with early-onset preeclampsia: A first look
preeclampsia is characterized by intense inflammatory response and an anti-angiogenic state. Maternal obesity has been considered to have important impact on the genesis of preeclampsia as lipotoxicity leads to maternal endothelial dysfunction and chronic inflammation. Here we investigate the plasma lipid profile of preeclamptic women.
Heading 6
Lipidomic Assessment of Plasma and Placenta of Women with Early-Onset Preeclampsia
Adipose tissue is responsible for triggering chronic systemic inflammatory response and these changes may be involved in the pathophysiology of preeclampsia.
Heading 6
The SURMetaGIT study: Design and rationale for a prospective pan-omics examination of the gastrointestinal response to Roux-en-Y gastric bypass surgery
To describe the protocol of the SURgically induced Metabolic effects on the Human GastroIntestinal Tract (SURMetaGIT) study, a clinical pan-omics study exploring the gastrointestinal tract as a central organ driving remission of type 2 diabetes mellitus (T2DM) after Roux-en-Y gastric bypass (RYGB). The main points considered in the study’s design and challenges faced in its application are detailed.
Heading 6
Correction: Plasma Metabolomics Biosignature According to HIV Stage of Infection, Pace of Disease Progression, Viremia Level and Immunological Response to Treatment
Scarpelini B, Zanoni M, Sucupira MCA, Truong H-HM, Janini LMR, Segurado IDC, et al. (2016) Plasma Metabolomics Biosignature According to HIV Stage of Infection, Pace of Disease Progression, Viremia Level and Immunological Response to Treatment. PLoS ONE 11(12): e0161920. pmid:27941971
Heading 6
The effect of coffee intake on lysophosphatidylcholines: A targeted metabolomic approach
Lysophosphatidylcholines (lysoPC) are known to be a pathological component of oxidized-LDL, and several studies demonstrate its pro-inflammatory properties in vitro. Nevertheless, bioactive compounds found in coffee, such as phenolic acids might inhibit LDL oxidation. The relationship between coffee consumption and lysoPC has not been described previously in humans. The aim of the present study was to assess the association between coffee intake and plasma lysoPC levels in adults.
Heading 6
Impaired branched-chain amino acid metabolism may underlie the nonalcoholic fatty liver disease-like pathology of neonatal testosterone-treated female rats
Polycystic ovary syndrome (PCOS) is frequently associated with non-alcoholic fatty liver disease (NAFLD), but the mechanisms involved in the development of NAFLD in PCOS are not well known. We investigated histological changes and metabolomic profile in the liver of rat models of PCOS phenotype induced by testosterone or estradiol. Two-day old female rats received sc injections of 1.25 mg testosterone propionate (Testos; n = 10), 0.5 mg estradiol benzoate (E2; n = 10), or vehicle (control group, CNT; n = 10). Animals were euthanized at 90–94 d of age and the liver was harvested for histological and metabolomic analyses. Findings showed only Testos group exhibited fatty liver morphology and higher levels of ketogenic and branched-chain amino acids (BCAA). Enrichment analysis showed effects of testosterone on BCAA degradation pathway and mitochondrial enzymes related to BCAA metabolism. Testos group also had a decreased liver fatty acid elongase 2 (ELOVL2) activity. E2 group had reduced lipid and acylcarnitine metabolites in the liver. Both groups had increased organic cation transporters (SLC22A4 and SLC16A9) activity. These findings indicate that neonatal testosterone treatment, but not estradiol, produces histological changes in female rat liver that mimic NAFLD with testosterone-treated rats showing impaired BCAA metabolism and dysfunctions in ELOVL2, SLC22A4 and SLC16A9 activity.
Heading 6
Efficacy of oral metformin in a patient with metastatic adrenocortical carcinoma: Examination of mechanisms and therapeutic implications
Although rare, adrenocortical carcinoma is among the most common tumors found in children with Li-Fraumeni syndrome and Li-Fraumeni-like syndrome, associated with germ-line mutations in the TP53 gene. In southern Brazil, one form of Li-Fraumeni syndrome, associated with childhood adrenocortical carcinoma, is caused by a mutation in the R337H TP53 tetramerisation domain and is attributed to a familial founder effect. Adrenocortical carcinoma is considered an aggressive neoplasm, usually of poor prognosis and is generally unresponsive to systemic chemotherapy. Optimal treatment regimens remain to be established. We report the case of a young woman with metastatic adrenocortical carcinoma, who achieved stable disease with mitotane, cisplatin, doxorubicin, and etoposide as first-line therapy, but then had an objective response to oral metformin that lasted 9 months. The presence of the R337H TP53 mutation suggests a mechanism for the observed response to metformin.
Heading 6
Analysis of the Lipid Profile in Patients with Colorectal Cancer in Advanced Stages
Colorectal (CRC) is one of the main cause of cancer worldwide. The search for noninvasive markers for diagnosis and monitoring as the use of analytical technologies such as mass spectrometry (MS), which allowed the search for lipid metabolites as candidates for probable biomarkers are needed.
Heading 6
Is Lipidomic the Answer to the Search of a Biomarker for Organ Preservation Protocol in Head and Neck Squamous Cell Carcinoma?
In the last decade organ preservation protocols
based on chemoradiotherapy (CRT) has been showing the
possibility of preserving function without jeopardizing survival for locally advanced head and neck squamous cell carcinoma (HNSCC). Still, only a percentage of the patients will
benefit from this approach and, to date, no biomarkers are
known to correctly predict these patients. More recently, modern mass spectrometry method has been used to determine
metabolic profiles, and lipidomics, in particular, emerged as
a new field of study in oncology and other diseases. This study
aimed to analyze the lipid profile on saliva from patients undergoing to a prospective, single center, open-label, nonrandomized phase II trial for organ preservation on HNSCC.
The lipid analysis was performed using matrix-assisted laser
desorption/ionization-time of flight mass spectrometry
(MALDI-TOF-MS). Multivariate statistical analyses based
on principal component analysis and orthogonal partial least
square-discriminant analysis were applied to MALDI-TOFMS data to visualize differences between the lipid profiles
and identify potential biomarkers. The results assisted on
distinguishing complete responders from non-responders to
the treatment protocol. In conclusion, we demonstrated that
a group of lipids is differentially abundant in saliva from
HNSCC patients submitted to an organ preservation protocol,
being able to differentiate responders from non-responders.
These results suggest the potential use of lipid biomarkers to
identify patients who may benefit from this treatment. Also,
we showed that saliva testing might be routinely used in clinical practice, for being a non-invasive alternative to blood
testing, besides inexpensive and easy to obtain.
Heading 6
RESEARCH ABSTRACTS
Brazilian Society of Clinical Oncology (SBOC)
19th Brazilian Congress of Clinical Oncology 2015
-
D’Amora P, Silva IDCG, Salzgeber MB, Girão MJBC, Kleine JPFO, Forde G, Bristow R, DiSaia PJ, Evans S, Nagourney RA. A phase II study in epithelial ovarian cancer (EOC) to correlate drug sensitivity and metabolic signatures with objective response (OR), time to progression (TTP), and overall survival (OS). Annals of the Brazilian Congress of Clinical Oncology (SBOC), Foz do Iguaçú, Paraná, Brazil, 2015.
American Society of Clinical Oncology (ASCO)
2013 – ASCO Annual Meeting
-
Colacino-Silva F, Maluf FC, Buzaid AC, Nagourney RA, Yamaguchi NH, D'Amora P, Evans S, Bernard PJ, Francisco F. International collaboration in personalized medicine for the treatment of advanced and drug-refractory cancers: Clinical application of human tumor primary culture analyses. J Clin Oncol 31, 2013 (suppl; abstr e13562). doi:10.1200/jco.2013.31.15_suppl.e13562.
2014 – ASCO Annual Meeting
-
Nagourney RA, Gansl RC, Lopes G, Buzaid AC, Maluf FC, D'Amora P, Yamaguchi NH, Colacino-Silva F, Mello AN. Cost benefit analysis of laboratory directed chemotherapy for advanced pancreatic cancer in U.S. and Brazilian patients. J Clin Oncol 33, 2015 (suppl; abstr e17782).
2015 – ASCO Annual Meeting
-
Nagourney RA, Bernard PJ, Francisco FR, Nagourney A, Evans S, Deo EA, D’Alpino RP. Metformin activity in advanced adrenocortical carcinoma: A comparative analysis in human tumors. J Clin Oncol 36, 2018 (suppl; abstr e14568). doi: 10.1200/JCO.2018.36.15_suppl.e14568.
2016 - American Association for Cancer Research (AACR). The Rivkin Center for Ovarian Cancer & the American Association for Cancer Research (AACR). 11th Biennial Ovarian Cancer Research Symposium – September 12-13, 2016. University of Washington, Seattle, Washington.
-
D’Amora P, Silva IDCG, Salzgeber MB, Girão MJBC, Bristow RE, Evans SS, DiSaia PJ, Nagourney RA. Correlation between drug sensitivity and metabolic signatures with objective response (OR), time to progression (TTP), and overall survival (OS) in advanced epithelial ovarian cancer (EOC): a phase II study. Proceedings of 11th Biennial Ovarian Cancer Research Symposium, poster TME&E-021, page 138. Winner of AACR-Aflac, Inc. Scholar-In-Training Award.
2017 - AACR International Conference & the Latin American Cooperative Oncology Group (LACOG) – May 4-6, 2017, São Paulo, Brazil.
-
D’Amora P, Silva IDCG, Salzgeber MB, Girão MJBC, Bristow RE, Evans SS, DiSaia PJ, Nagourney RA. Metabolic signatures in patients with advanced epithelial ovarian cancer: correlation with clinical response parameters in a phase II study. Proceedings of AACR & LACOG International Conference, poster session B, page 82. Winner of AACR-LACOG Scholar-In-Training Award.
2022 - AACR Annual Meeting – April 4-6, 2022, New Orleans, Louisiana.
-
Complete remission in advanced epithelial ovarian cancer is predicted by metabolic signatures measured in the media of patient’s primary culture 3D tumor explants: A metabolomic analysis. Adam J. Nagourney, Paulo D'Amora, Ismael Dale Cotrim Guerreiro Silva, Steven S. Evans, Robert A. Nagourney. Nagourney Cancer Institute, Long Beach, CA, Federal University of São Paulo, São Paulo, Brazil, Rational Therapeutics, LLC, Long Beach, CA.
Link: https://www.abstractsonline.com/pp8/#!/10517/presentation/12833
2022 – ASCO Annual Meeting – June 3-7, 2022, Chicago, Illinois.
-
Drugging the Undruggable-Targeting P53: A Comparative Analysis of APR-246 and COTI-2 in human tumor primary culture explants. Adam Jeremiah Nagourney, Steven Scott Evans, Max Serge Duesberg, Paulo D'Amora, Paula J. Bernard, Eric Francisco, Robert Alan Nagourney. J Clin Oncol 40, 2022 (suppl 16; abstr e15092). DOI: 10.1200/JCO.2022.40.16_suppl.e15092. Abstract #: e15092.