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BioWorld - Friday, May 8, 2026
Home » Topics » Biomarkers, BioWorld Science

Biomarkers, BioWorld Science
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Illustration of magnifying glass inspecting brain
Neurology/psychiatric

Anchoring, and bootstrapping, psychiatry into the precision medicine era

Nov. 4, 2025
By Anette Breindl
No Comments
Psychiatry has struggled to enter the precision medicine era. But through a mix of innovations and bootstrapping, progress is coming to the field. Scientists are working on improving diagnoses by investigating potential biomarkers and collection methods.
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Illustration of women's reproductive organs
Biomarkers

Biomarker panel of three serum microRNAs predicts cervical cancer prognosis

Oct. 28, 2025
No Comments
MicroRNAs (miRNAs) play key roles in cancer development by regulating genes involved in cell growth, differentiation, invasion, metastasis and angiogenesis. Because their expression patterns differ across tumor types and stages, miRNA profiles hold strong potential as noninvasive diagnostic and prognostic biomarkers.
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Illustration of RNA strands in red and white
Biomarkers

LINC01354 is a prognostic marker in esophageal cancer

Oct. 23, 2025
No Comments
Esophageal cancer is among the most lethal cancers with a high mortality rate worldwide. Chinese researchers have explored the potential link between long intergenic non-protein coding RNA 1354 (LINC01354) and esophageal cancer.
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Biomarkers

FGF5 gene involved in excessive hair growth

Oct. 22, 2025
No Comments
Hirsutism is the excessive hair growth in women in male-typical areas, usually associated with androgen excess and other conditions such as polycystic ovary syndrome (PCOS). The genetic basis of hirsutism remains poorly understood; researchers from the University of Oulu and collaborators performed a meta-analysis of genome-wide association studies from 4,834 cases of hirsutism and 352,966 controls across three cohorts.
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Neurology/psychiatric

Study identifies REST as biomarker and siRNA target in ALS

Oct. 21, 2025
No Comments
Restrictive element-1 silencing transcription factor (REST) has key roles in neuronal differentiation, structural remodeling and plasticity, contributing to neuronal homeostasis in postnatal neurons. It acts as a suppressor of neuronal gene expression in stem and progenitor cells, and abnormal accumulation of it has been linked to several neurological disorders, like Huntington’s disease, epilepsy and stroke.
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Biomarkers

New link between PRRX1 gene and open-angle glaucoma

Oct. 21, 2025
No Comments
Primary open-angle glaucoma (POAG) is among the leading causes of irreversible blindness. Early detection and treatment are crucial for vision preservation, and research to identify genes associated with POAG is ongoing.
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Purple-tinted test tubes and dropper
Biomarkers

miR-1265 emerges as a biomarker of meningioma

Oct. 17, 2025
No Comments

Meningiomas are usually grade I benign tumors that can turn into aggressive grade II or III malignant tumors. Genome-wide methylation analysis has shown that microRNA 1265 (miR-1265) is hypermethylated in meningiomas.


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Fallopian tubes, ovaries and uterus
Biomarkers

AKR1B1 and AKR1B10 as prognostic markers in endometrial cancer

Oct. 17, 2025
No Comments
Endometrial cancer is the most prevalent gynecological malignancy in high-income countries, and the discovery of new biomarkers may aid in earlier detection and improve the prognosis of patients.
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Respiratory

MFAP5: Potential biomarker of interstitial lung disease

Oct. 17, 2025
No Comments
To identify potential biomarkers of interstitial lung disease, researchers at West China Hospital of Sichuan University and Minda Hospital of Hubei Minzu University mined the Gene Expression Omnibus database of transcriptomes as well as compared tissues across healthy individuals and patients with connective tissue disease, who had interstitial lung disease or not.
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Illustration of DNA, magnifying glass
Genetic/congenital

Study identifies three new genes linked to cleft lip, palate risk

Oct. 16, 2025
No Comments
A recent study published in PLOS Genetics has identified several novel genetic variants associated with the risk of orofacial clefts, a common and complex congenital disability. Orofacial clefts are caused by a combination of genetic and environmental factors and can occur in isolation or simultaneously with other birth defects.
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