# ALDH1 and ALCAM as emerging biomarkers in personalized rectal cancer therapy

**Authors:** Jurandir Marcondes RIBAS-FILHO, Efstathia N DOELKEN, Sudipta TRIPATHI, Bülent POLAT, Reinhard LISSNER, Thomas BÖELDICKE, Carmen Austrália Paredes Marcondes RIBAS, Osvaldo MALAFAIA, Martin GASSER, Ana Maria WAAGA-GASSER

PMC · DOI: 10.1590/0102-67202025000051e1920 · Arquivos Brasileiros de Cirurgia Digestiva : ABCD · 2026-02-16

## TL;DR

The study explores ALDH1 and ALCAM as potential biomarkers in rectal cancer, finding elevated levels in patients but limited correlation with tumor stage or survival.

## Contribution

The study investigates ALDH1 and ALCAM as novel serum biomarkers for rectal cancer prognosis and therapy monitoring.

## Key findings

- Serum levels of ALCAM and ALDH1 were elevated in rectal cancer patients compared to healthy controls.
- No significant correlation was found between biomarker levels and tumor stage or patient survival.
- Biomarker expression in tumor tissues increased with advanced UICC stages.

## Abstract

The preoperative evaluation of serum tumor markers provides valuable prognostic and therapeutic insights in solid malignancies. Although not diagnostic by themselves, increased preoperative concentrations often reflect greater tumor burden, advanced disease stage, and unfavorable clinical outcomes.

The aim of this study was to investigate the expression and diagnostic-prognostic potential of the tumor markers aldehyde dehydrogenase 1 (ALDH1) and activated leukocyte cell adhesion molecule (ALCAM) in the blood of rectal cancer patients under the influence of short- or long-term radio-/chemoradiotherapy (RTx/RCTx).

Serum samples taken from patients with rectal carcinoma (n=164) at different time points during and after RTx/RCTx were retrospectively examined to determine whether these markers could predict disease progression and long-term survival.

Kaplan-Meier analysis confirmed the prognostic relevance of the Union for International Cancer Control (UICC) staging, while no significant associations were observed between serum levels of the investigated biomarkers and individual patient or tumor characteristics such as age, sex, or tumor stage. Overall, ALCAM and ALDH1 in this limited patient cohort exhibited elevated serum levels compared with healthy controls, and tumor tissues demonstrated stage-dependent increases in marker expression (UICC III/IV versus I/II).

Serum concentrations of ALCAM and ALDH1 were significantly elevated in our patient cohort with rectal cancer but showed no significant correlation with tumor stage or survival, whenever serum samples were obtained either during or after neoadjuvant and adjuvant therapy, which may be particularly due to the limited number of studied subjects. Although their prognostic utility remains limited, their consistent elevation in cancer patients underscores their potential value in early detection or as components of a broader biomarker panel.

Rectal cancer continues to represent a major public health issue worldwide, with incidence rising progressively with advancing age.

The preoperative evaluation of serum tumor markers offers significant prognostic and therapeutic insights in patients with solid neoplasms.

Carcinoembryonic Antigen (CEA) remains a well-established prognostic indicator in colorectal cancer.

Cancer stem cells (CSCs) have emerged as pivotal elements in the onset, progression, and recurrence of malignant tumors.

Multiple markers have been proposed in CRC as indicative of CSC activity, including CD44, CD24, CD133, CD166, ALCAM, EpCAM, LGR5, and ALDH1.

Rectal cancer is a major global health concern, with incidence increasing alongside aging populations. Although the overall 5-year survival rate is only slightly higher than that of colon cancer, stage-specific outcomes remain comparable between the two entities. Nevertheless, patients with rectal carcinoma exhibit a greater propensity for locoregional recurrence and, in many cases, distant metastatic spread, despite continuous advances in multimodal treatment strategies.

The evaluation of serum biomarkers such as aldehyde dehydrogenase 1 (ALDH1) and activated leukocyte cell adhesion molecule (ALCAM) offers new insights into the biological behavior of rectal cancer. Their analysis may contribute to refining prognostic assessment and therapeutic monitoring, ultimately advancing the development of more individualized approaches for patients undergoing neoadjuvant and adjuvant therapies.

## Linked entities

- **Genes:** ALDH1A1 (aldehyde dehydrogenase 1 family member A1) [NCBI Gene 216], ALCAM (activated leukocyte cell adhesion molecule) [NCBI Gene 214], CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960], CD24 (CD24 molecule) [NCBI Gene 100133941], PROM1 (prominin 1) [NCBI Gene 8842], ALCAM (activated leukocyte cell adhesion molecule) [NCBI Gene 214], EPCAM (epithelial cell adhesion molecule) [NCBI Gene 4072], LGR5 (leucine rich repeat containing G protein-coupled receptor 5) [NCBI Gene 8549]
- **Diseases:** rectal cancer (MONDO:0006519), colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** EPCAM (epithelial cell adhesion molecule) [NCBI Gene 4072] {aka Ber-Ep4, BerEp4, DIAR5, EGP-2, EGP314, EGP40}, LGR5 (leucine rich repeat containing G protein-coupled receptor 5) [NCBI Gene 8549] {aka FEX, GPR49, GPR67, GRP49, HG38}, ALCAM (activated leukocyte cell adhesion molecule) [NCBI Gene 214] {aka CD166, MEMD}, ALDH1A1 (aldehyde dehydrogenase 1 family member A1) [NCBI Gene 216] {aka ALDC, ALDH-E1, ALDH1, ALDH11, HEL-9, HEL-S-53e}, CD24 (CD24 molecule) [NCBI Gene 100133941] {aka CD24A}, PROM1 (prominin 1) [NCBI Gene 8842] {aka AC133, CD133, CORD12, MCDR2, MSTP061, PROML1}, CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960] {aka CDW44, CSPG8, ECM-III, ECMR-III, H-CAM, HCELL}
- **Diseases:** prostate, esophageal, breast, and urothelial carcinomas (MESH:D001943), lymph node (MESH:D000072717), ovarian malignancies (MESH:D010051), gastrointestinal tumors (MESH:D005770), nodal (MESH:D013611), metastases (MESH:D009362), CRC (MESH:D015179), esophageal, breast, lung, stomach, and ovarian cancers (MESH:D061325), death (MESH:D003643), colonic tumors (MESH:D003110), cancer antigen-125 (MESH:D009369), Rectal cancer (MESH:D012004), rectal lesion (MESH:D012002), melanoma (MESH:D008545), ABCD (MESH:C535334)
- **Chemicals:** eosin (MESH:D004801), DAPI (MESH:C007293), AlexaFluor 488 (MESH:C000711379), acetone (MESH:D000096), H.E. (MESH:D006371), Cy3 (-), hematoxylin (MESH:D006416), aldehydes (MESH:D000447), RTx (MESH:C024353), oxaliplatin (MESH:D000077150), 5-FU (MESH:D005472), TBS (MESH:D013725), methanol (MESH:D000432)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12919921/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12919921/full.md

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Source: https://tomesphere.com/paper/PMC12919921