ClinicalTrials.Veeva

Menu

Folate One-carbon Malnutrition as the Metabostemness Risk Factor of Malignancy Tumor Development of NSCLC Patients

National Taiwan University logo

National Taiwan University

Status

Unknown

Conditions

Lung Cancer, Nonsmall Cell

Treatments

Behavioral: nutrition consult

Study type

Observational

Funder types

Other

Identifiers

NCT03504098
201701123RINC

Details and patient eligibility

About

Non-small cell lung cancer (NSCLC) accounts for more than two-thirds of lung cancer, which is the leading cause of cancer deaths in Taiwan. The overall prognosis of NSCLC is poor with low 5-year survival rates. Recent advances suggest that malignancy NSCLC cancers are the cancer stem cell (CSC) diseases. The stemness potentials of CSC with epithelial-mesenchymal transdifferentiation ensure their invasion and disseminate to metastsis organs. The self-renewal property of CSC mediates intrinsic drug resistance to cytotoxicity therapy and promoted aggressive relapse tumour. Metabolic reprogramming on bioenergetics of malignant cancer cells has been proposed as the key mediator in the stemness CSC development. Malignancy cells uptake glucose for fermented glycolysis to produce lactate which release resulted in acidified microenvironment to trigger the mTOR and sonic hedgehog metabolic stress signaling in supporting CSC stemness potentials. The metabostemness of cancer cells is the new-dimensional hallmark of malignancy tumour, which may serve as the diagnostic markers for the early detection of malignancy cancers. Folate-mediated one carbon metabolism coordinates glucose into amino acid metabolism to tailor the fuel metabolites in supporting macromolecule synthesis and to sustain the bioenergetics requirement. Acting as the metabolic stressor, low folate intake is associated with increased risks of lung cancers. Folate and one-carbon nutrient status of NSCLC patients in Taiwan, however, has not been assessed. The role of low folate metabolic stress (LFMS) in metabostemness marker and metastasis potentials of malignancy NSCLC is unexplored. The causal effect and the working mechanisms by which LFMS promoted NSCLC malignancy remain elusive.

Enrollment

300 estimated patients

Sex

All

Ages

20 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Surgeon diagnosed as the first time having non-small cell lung cancer from the surgical clinic of National Taiwan University Hospital

Exclusion criteria

  • Patients Suffer from major diseases such as heart, liver, kidney, or peripheral arterial disease, or having mental illness
  • Diabetes and non-lung cancer patients
  • Pregnancy, breast-feeding pregnant women

Trial design

300 participants in 3 patient groups

Lung cancer patients tumor
Description:
Using to analysis metabolomic markers, one carbon folate nutrition levels in lung cancer patients.
Lung cancer patients blood
Description:
Using to analysis folate, B12, homocysteine levels in plasma and RBC. Using to analysis cDNA gene test in buffy coat.
Treatment:
Behavioral: nutrition consult
Lung cancer patients
Description:
Supply nutrition counseling
Treatment:
Behavioral: nutrition consult

Trial contacts and locations

1

Loading...

Central trial contact

Rwei-Fen S.Huang; Jin-Shing Chen

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems