# Expression Patterns and Clinical Relevance of HSP70 and Metallothionein in Triple-Negative and Luminal A Breast Cancer: A Croatian Cohort Study

**Authors:** Sara Bilić Knežević, Tamara Gulić, Damir Grebić, Mirisa Tokić, Manuela Avirović, Anita Savić-Vuković, Marin Marinović, Davor Jurišić, Dalibor Broznić

PMC · DOI: 10.3390/cells15040351 · Cells · 2026-02-15

## TL;DR

The study finds that HSP70 and metallothionein expression patterns in breast cancer reflect cellular stress adaptation but are not reliable predictors of patient outcomes.

## Contribution

The study provides new insights into the role of HSP70 and metallothionein in breast cancer subtypes, emphasizing their biological relevance over prognostic value.

## Key findings

- Nuclear HSP70 expression is significantly higher in malignant breast cancer compared to benign lesions.
- Cytoplasmic metallothionein expression is significantly lower in TNBC and Luminal A carcinomas.
- HSP70 and metallothionein expression does not independently predict clinical outcomes in breast cancer.

## Abstract

What are the main findings?
Nuclear expression of HSP70 is significantly higher in malignant breast cancer specimens than in benign lesions, regardless of molecular subtype.Cytoplasmic expression of metallothionein is significantly lower in TNBC and Luminal A carcinomas, without independent prognostic value.

Nuclear expression of HSP70 is significantly higher in malignant breast cancer specimens than in benign lesions, regardless of molecular subtype.

Cytoplasmic expression of metallothionein is significantly lower in TNBC and Luminal A carcinomas, without independent prognostic value.

What are the implications of the main findings?
HSP70 and metallothionein expression patterns reflect cellular adaptation to stress rather than serving as independent prognostic biomarkers in breast cancer.The results emphasize the importance of protein subcellular localization and an integrative approach in breast cancer biomarker research.

HSP70 and metallothionein expression patterns reflect cellular adaptation to stress rather than serving as independent prognostic biomarkers in breast cancer.

The results emphasize the importance of protein subcellular localization and an integrative approach in breast cancer biomarker research.

Metallothioneins (MTs) and heat shock protein 70 (HSP70) are key regulators of cellular stress response and metal homeostasis and play important roles in tumor biology. The aim of this study was to examine their expression patterns and potential prognostic significance in different molecular subtypes of breast cancer (BC), with special emphasis on triple-negative breast cancer (TNBC) and the Luminal A subtype, compared with benign breast lesions (fibroadenomas). A total of 90 tissue samples were included, and the expression of MTs in the cytoplasm and nucleus and HSP70 in the nucleus of tumor cells was analyzed immunohistochemically and correlated with clinicopathological features and treatment outcomes. Distinct expression patterns of HSP70 and MTs were observed between malignant and benign samples, as well as among the analyzed molecular subtypes of BC, suggesting their involvement in cellular adaptive mechanisms associated with malignant transformation. TNBC was characterized by less favorable clinicopathological features compared to the Luminal A subtype, including higher histological grade, increased proliferative activity, and a higher incidence of recurrence and metastatic disease. Survival analyses confirmed a worse outcome for patients with TNBC, while HSP70 and MTs expression did not show independent prognostic value in multivariate models. In conclusion, although HSP70 and MTs play important biological roles in the cellular response to stress and tumor adaptation, their expression in this study does not represent an independent prognostic indicator of clinical outcome. Nevertheless, the observed expression patterns provide insight into the complex mechanisms of tumor adaptation and emphasize the need for integrative approaches in BC biomarker research.

## Linked entities

- **Proteins:** HSPA1A (heat shock protein family A (Hsp70) member 1A)
- **Diseases:** Triple-Negative Breast Cancer (MONDO:0005494), Luminal A Breast Cancer (MONDO:0021116), breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, MTF1 (metal regulatory transcription factor 1) [NCBI Gene 4520] {aka MTF-1, ZRF}, HSPA4 (heat shock protein family A (Hsp70) member 4) [NCBI Gene 3308] {aka APG-2, HEL-S-5a, HS24/P52, HSPH2, RY, hsp70}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, FOXP3 (forkhead box P3) [NCBI Gene 50943] {aka AIID, DIETER, IPEX, JM2, PIDX, XPID}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, MLRL (Myeloid leukemia-related gene (myeloid tumor suppressor)) [NCBI Gene 8201] {aka MLRG, MTS}, TWIST1 (twist family bHLH transcription factor 1) [NCBI Gene 7291] {aka ACS3, BPES2, BPES3, CRS, CRS1, CSO}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, SNAI1 (snail family transcriptional repressor 1) [NCBI Gene 6615] {aka SLUGH2, SNA, SNAH, SNAIL, SNAIL1, dJ710H13.1}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, MT3 (metallothionein 3) [NCBI Gene 4504] {aka GIF, GIFB, GRIF, ZnMT3}
- **Diseases:** node (MESH:D012804), fibrosis (MESH:D005355), PHD (MESH:D011547), injury to (MESH:D014947), Luminal A carcinoma (MESH:D009369), carcinoma of no special type (MESH:D012678), medullary and metaplastic carcinomas (MESH:D018276), carcinogenesis (MESH:D063646), FA (MESH:D018226), hypoxia (MESH:D000860), Non-special type (NST) carcinoma (MESH:D002289), Metastases (MESH:D009362), DFS (MESH:D011475), death (MESH:D003643), benign breast lesions (MESH:D061325), tumorigenic (MESH:D002471), in situ (MESH:D000093284), invasive lobular carcinoma (MESH:D018275), cytotoxic (MESH:D064420), TNBC (MESH:D064726), BC (MESH:D001943), TNM (MESH:D008207), lymph node (MESH:D000072717), ductal carcinoma (MESH:D044584), poorly differentiated (MESH:D020522), invasive tumors (MESH:D009361), cysts (MESH:D003560)
- **Chemicals:** metal (MESH:D008670), zinc (MESH:D015032), Alexa Fluor 594 (-), Alexa Fluor 488 (MESH:C000711379), ATP (MESH:D000255), ROS (MESH:D017382), 4',6-diamidino-2-phenylindole (MESH:C007293), Formalin (MESH:D005557)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

72 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938892/full.md

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Source: https://tomesphere.com/paper/PMC12938892