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miR-155 overexpression is frequently associated with treatment resistance across 8 cancer typesmiR-155 Expression Linked to Treatment Resistance in Various Cancers

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Key Takeaway
Note that miR-155 overexpression is frequently associated with treatment resistance across multiple cancer types.

This systematic review synthesizes evidence from 19 studies across 8 cancer types, including breast cancer, non-small cell lung cancer, and cutaneous melanoma, to evaluate the role of microRNA-155 (miR-155) in clinical outcomes. The primary focus was the relationship between miR-155 expression and treatment sensitivity or resistance.

The authors found that most studies associated miR-155 overexpression with treatment resistance. Conversely, only a few studies reported an association between elevated miR-155 expression and enhanced treatment sensitivity. These findings suggest a complex role for miR-155, though the evidence for sensitivity is less consistent than the evidence for resistance.

Limitations of the review include a search restricted to only three databases and a limited 5-year timeframe. These constraints may impact the comprehensiveness of the findings. The authors conclude that the prognostic and predictive significance of miR-155 warrants further evaluation before it can be used as a definitive biomarker. Clinical application is currently limited by the need for more extensive research to clarify the role of miR-155 in specific cancer types.

How this fits prior evidence

This systematic review addresses a gap in the understanding of molecular biomarkers for cancer prognosis. While prior coverage noted that integrating clinical and genomic data may improve progression risk prediction in advanced breast cancer, this review specifically examines the role of miR-155 in 8 different cancer types. The findings regarding miR-155 and treatment resistance provide a specific molecular focus that complements the broader genomic integration strategies previously discussed.

A systematic review looked at 19 studies involving eight different types of cancer, including lung, breast, and thyroid cancers. The researchers focused on a molecule called microRNA-155 (miR-155) to see how its presence relates to patient outcomes and treatment success.

The findings showed that in most cases, high levels of miR-155 were associated with treatment resistance. This means the cancer was harder to treat. However, a small number of studies reported that higher levels of miR-155 were linked to better treatment sensitivity in some instances.

Because this review only looked at a small number of studies from a short timeframe, the results are not definitive. The findings show a link between miR-155 and treatment outcomes, but they do not prove that miR-155 causes these results. More research is needed to understand if this molecule can reliably predict how a patient will respond to therapy.

What this means for you:
Higher miR-155 levels are often linked to treatment resistance, but more research is needed to confirm this link.

Common questions

What is miR-155 and how does it affect cancer treatment?

miR-155 is a molecule that researchers studied in relation to cancer treatment. The review of 19 studies found that high levels of miR-155 were associated with treatment resistance in most cases. This means the cancer was harder to treat. However, a few studies showed it could be linked to better treatment sensitivity.

Which types of cancer were studied in relation to miR-155?

The review included 19 studies covering eight different types of cancer. These included breast cancer, non-small cell lung cancer, pediatric acute lymphoblastic leukemia, cutaneous melanoma, non-muscle-invasive bladder cancer, papillary thyroid cancer, pancreatic ductal adenocarcinoma, and diffuse large B-cell lymphoma.

Can miR-155 be used to predict if a treatment will work?

While the study found a link between miR-155 and treatment resistance, the results are not yet enough to use it as a definitive biomarker. The researchers noted that the role of miR-155 in predicting treatment outcomes needs more evaluation before it can be used in clinical practice.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedOct 2026
View Original Abstract ↓
BackgroundOverexpression of microRNA-155 (miR-155) has been associated with cancer development, metastasis, and possible drug resistance. This systematic review analyzed the evidence from the existing literature on miR-155 expression in cancer patients undergoing treatment.MethodsA thorough literature search was conducted in databases and search engines (ProQuest, PubMed, and Google Scholar) from January 2019 to December 2024 to identify clinical evidence on miR-155 expression in cancer treatments. To assess miR-155 expression in relation to clinical outcomes, we included 15 cancers in this systematic review. Following the PRISMA 2020 guidelines, three independent reviewers selected, extracted, and assessed the data against the predefined inclusion criteria, and a fourth reviewer verified the assessments and resolved discrepancies.ResultsOf the 15 cancers analyzed, 19 eligible studies covering eight cancers were identified and included in the review, namely breast cancer, non-small cell lung cancer, pediatric acute lymphoblastic leukemia, cutaneous melanoma, non-muscle-invasive bladder cancer, papillary thyroid cancer, pancreatic ductal adenocarcinoma, and diffuse large B-cell lymphoma. Screening and evaluation of these 19 studies showed that miR-155 expression varied by cancer type, treatment strategy, and patient sample type. While most studies associated miR-155 overexpression with treatment resistance, a few reported an association between elevated miR-155 expression and enhanced treatment sensitivity. A limitation of this study is that the search for studies reporting miR-155 expression in relation to therapeutic outcomes in patients with cancer was restricted to three databases and a 5-year timeframe.ConclusionOverall, the results of this study indicate that the prognostic and predictive significance of miR-155 warrants further evaluation.Systematic Review RegistrationPROSPERO ID, CRD42025632573.
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