PIPages
Labs

Analisa DiFeo

University of Michigan, MI·Medicine & Clinical Research

High grade serous carcinoma (HGSC), the most common type of ovarian cancer, is among the deadliest cancers in women. This is largely because tumors return and stop responding to chemotherapy.

Fields

Medicine & Clinical Research

Microbiology & Immunology

Genetics

Topics

ovarian cancer

high grade serous carcinoma

miR-181a

Grants
1 known grant, through Mar 2028

What they work on

  1. Determine how loss of the microRNA miR-181a affects immune cell infiltration and interferon signaling in patient-derived ovarian tumor organoids, with and without a STING agonist or anti-PD-L1 immunotherapy.
  2. Test in vivo whether miR-181a levels change ovarian tumors' sensitivity to STING agonists or anti-PD-L1 treatment.
  3. Assess whether activating miR-181a, alone or together with loss of various tumor suppressor genes, is sufficient to drive tumor formation in mice.

More about the research

Immunotherapies that unleash the immune system have so far failed in HGSC, mostly because these tumors build a strongly immunosuppressive environment. A main way tumors do this is by shutting down STING (Stimulator of Interferon Genes). STING detects stray DNA inside cells and switches on interferon signaling, an antiviral-style alarm that attracts immune attack.

Why it matters

Women with high grade serous ovarian cancer have few effective options once tumors recur or resist chemotherapy, and current immunotherapies largely fail. If blocking miR-181a can reactivate STING-driven immune signaling, combining it with STING agonists or anti-PD-L1 drugs could become a strategy to make these tumors respond to immune-based treatment.

Known grants

From NIH and NSF research grants. Labs often have other funding we can't see.

Examining the role of the miR-181a:Wnt/B-catenin axis in ovarian cancer

NIH · Apr 2016 – Mar 2028

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Karen Swanson

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The school

University of Michigan: 124 labs on PI Pages, $2.1B a year on research, 963 research doctorates a year.

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