Study / S0BBCQFXK2026-05-07

TREND: A generalizable synthetic enhancer discovery platform for targeted immunotherapy

Yingbo Jia, Chu-Yen Chen, Bo Zhu, Zhigui Wu, Yi-Chia Wu et al.

About this study

Synthetic enhancers with high specificity are crucial for therapeutic gene control. However, experimental screens and machine learning-guided design typically require context-specific datasets, limiting generalizability. Because transcription factor (TF) activity reflects cellular state, TF-responsive enhancer libraries offer a universal starting point. Here, we developed TREND (transcription factor-responsive enhancer discovery), a massively parallel reporter assay of ~2.7 million enhancer-barcode constructs representing 57,715 designs. TREND covers 1,068 motif-annotated proteins, including 729 confirmed TFs across 49 DNA-binding domain families. Applied to ovarian cancer, TREND identified enhancers that discriminate cancer from normal epithelial cells. These enhancers enabled protein-interaction-based AND-gate circuits with reduced OFF-state leakage and amplified ON-state output, driving tumor-restricted expression of combinatorial immune effectors and robust antitumor responses in murine ovarian cancer models. TREND also identified T-cell activation-responsive enhancers with greater inducibility and lower basal activity than conventional NFAT-motif-based elements. Together, TREND provides a generalizable framework for context-specific enhancer discovery and therapeutic gene regulation.

Full author list & citation

Yingbo Jia, Chu-Yen Chen, Bo Zhu, Zhigui Wu, Yi-Chia Wu, Renqi Wang, Abdulmajeed I. Salamah, Sushmita Halder, Yen-Nien Liu, Yingjie Guo, Ying Chen, Luca Scimeca, Hang Yin, Tejas Sabu, Yutao Wang, Enoch B. Antwi, Yang Wang, Ming-Ru Wu. TREND: A generalizable synthetic enhancer discovery platform for targeted immunotherapy. 2026-05-07. https://doi.org/10.64898/2025.12.08.693012

Experiments 2

E1FVS7XW7

TREND synthetic enhancer screen in ovarian cancer and epithelial cell contexts

A pooled synthetic TF-binding-site enhancer library was delivered by lentivirus to human OVCAR-8 ovarian cancer cells (OV8), immortalized human ovarian surface epithelial cells (IOSE), and murine ID8 ovarian cancer cells. Enhancer activity was quantified from barcode-linked RNA/DNA ratios across three OV8 replicates, three IOSE replicates, and two ID8 replicates, with cancer-selective activity summarized relative to IOSE.

Integrated lentiMPRANot reported
Explore data
E2D1WAULR

TREND enhancer screen for primary human T-cell activation

A pooled synthetic TF-binding-site enhancer library was screened in primary human CD3-positive T cells from two independent donors. Barcode-linked reporter activity was compared between resting cells and cells restimulated through CD3/CD28, yielding donor-resolved activation ratios and a cross-donor summary.

Integrated lentiMPRAHuman
Explore data

Raw source data 11 files

Original supplemental and deposited inputs retained for this study. Download files individually or together as a ZIP; nested folders are preserved. Source reuse terms apply, and sequencing reads may be omitted.

Download all 11 files (ZIP)activation_responsive_enhancer_screening_result_donor1.csvactivation_responsive_enhancer_screening_result_donor2.csvall_enhancer_metadata_111525.csvovarian_cancer_project.yamlovarian_cancer_specific_enhancer_screening_analysis.Rovca_sensor_activity_result_all.csvovca_sensor_activity_result_concise.csvREADME.txtselected_T_cell_activation_inducible_enhancers_for_synthesis.xlsxT_cell_activation_project.yamlT_cell_activation_responsive_enhancer_screening_analysis.R

Cite OpenMPRA

Cite the OpenMPRA database. Include your access date because the collection changes over time.

Please also cite the source studies when using their data.