# pH‐Dependent Microenvironmental Ionic Signaling in Pancreatic Ductal Adenocarcinoma

**Authors:** Albrecht Schwab, Micol Rugi, Pawel Swietach, Wiktoria Błaszczak, Ivana Novak, Ganga Deshar, Stine Falsig Pedersen, Renata Ialchina, Albin Sandelin, Jiayi Yao, Stephan J. Reshkin, Rosa A. Cardone, Tiago M. A. Carvalho, Annarosa Arcangeli, Rayhana Bouazzi, Franco N. D'Alessandro, Natalia Prevarskaya, Madelaine M. Audero, Halima Ouadid‐Ahidouch, Julie Schnipper, Luis A. Pardo, Xiaoyi Shi, Frauke Alves, Jakub Mitręga, Anna Trauzold, Sofie E. Hagelund, György Panyi, Marco Cozzolino, Clemens M. W. G. Löwik, Laura Mezzanotte, Roisin McMorrow, Andreas Pahl, Torsten Hechler, Elena Papacharisi, Alessandra Fiorio Pla, Ildiko Szabo, Verena Hofschröer, Zoltán Pethő

PMC · DOI: 10.1111/apha.70183 · Acta Physiologica (Oxford, England) · 2026-02-27

## TL;DR

This paper explores how pH changes in the pancreas influence pancreatic cancer development and suggest targeting pH-regulating proteins as a potential treatment.

## Contribution

The paper highlights the novel role of pH-regulatory transport proteins in shaping the pancreatic cancer microenvironment and their potential as therapeutic targets.

## Key findings

- pH-regulatory transport proteins act as signaling hubs influencing cancer cell behavior and immune evasion.
- Inhibiting pH-regulatory proteins in mouse models impacts tumor immune defense and cancer-immune cell communication.
- These proteins, essential for normal pancreas function, are co-opted to support cancer progression.

## Abstract

Pancreatic ductal adenocarcinoma (PDAC) develops within a uniquely dynamic pH landscape shaped by substantial acid–base fluxes produced by the exocrine pancreas. Secretion of alkaline pancreatic juice, normally linked to digestion, produces intermittent acidifications of the pancreatic interstitium, which challenges epithelial and stromal cells. It was postulated that these unique pancreatic pH dynamics can facilitate PDAC initiation and progression through selection of a more aggressive phenotype emerging with PDAC driver mutations.

Here, we summarize evidence that pH‐regulatory transport proteins have an important role in shaping the PDAC microenvironment.

pH‐regulatory transport proteins generate and sense their microenvironment and act as signaling hubs to regulate proliferation, migration, and metabolism, and immune evasion. In this way, transport proteins that are crucial for the normal physiology of the exocrine pancreas are misused and become coerced into playing a pro‐cancer role in pancreatic tumor cells, pancreatic stellate cells, or infiltrating immune cells. Experiments with PDAC mouse models revealed a therapeutic potential of targeting pH dynamics, notably by inhibition or genetic ablation of pH‐regulatory proteins. It is a consistent finding that these maneuvers have a marked impact on the tumor immune defense and the communication between cancer and immune cells.

Collectively, we present a case for considering pH‐regulating proteins as a therapeutic avenue.

## Linked entities

- **Diseases:** pancreatic ductal adenocarcinoma (MONDO:0005184)

## Full-text entities

- **Genes:** Slc16a3 (solute carrier family 16 (monocarboxylic acid transporters), member 3) [NCBI Gene 80879] {aka Mct3, Mct4}, Kcnn4 (potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4) [NCBI Gene 16534] {aka IK1, IKCA1, KCA4, KCa3.1, SK4, SKCas}, Trpv4 (transient receptor potential cation channel, subfamily V, member 4) [NCBI Gene 63873] {aka 0610033B08Rik, OTRPC4, Trp12, VR-OAC, VRL-2, VROAC}, SLC4A7 (solute carrier family 4 member 7) [NCBI Gene 9497] {aka NBC2, NBC3, NBCN1, SBC2, SLC4A6}, Trpc1 (transient receptor potential cation channel, subfamily C, member 1) [NCBI Gene 22063] {aka Mtrp1, Trp1, Trrp1}, Car9 (carbonic anhydrase 9) [NCBI Gene 230099] {aka CAIX, Ca9, MN/CA9}, Ly6g (lymphocyte antigen 6 family member G) [NCBI Gene 546644] {aka Gr-1, Gr1, Ly-6G}, Pdx1 (pancreatic and duodenal homeobox 1) [NCBI Gene 18609] {aka IDX-1, IPF-1, Ipf1, Mody4, STF-1, pdx-1}, Cd69 (CD69 antigen) [NCBI Gene 12515] {aka 5830438K24Rik, AIM, VEA}, Trpv6 (transient receptor potential cation channel, subfamily V, member 6) [NCBI Gene 64177] {aka CAT, CaT1, Cac, Ecac2, Otrpc3}, Mcph1 (microcephaly, primary autosomal recessive 1) [NCBI Gene 244329] {aka 5430437K10Rik, BRIT1, D030046N04Rik, MCT, Tg(HLA-A2.1)1Enge}, Hc (hemolytic complement) [NCBI Gene 15139] {aka C5, C5a, He, Hfib2}, Cdkn2a (cyclin dependent kinase inhibitor 2A) [NCBI Gene 12578] {aka ARF-INK4a, Arf, INK4a-ARF, Ink4a/Arf, MTS1, Pctr1}, Slc9a1 (solute carrier family 9 (sodium/hydrogen exchanger), member 1) [NCBI Gene 20544] {aka Apnh, Mir5122, Nhe1, mir-5122, swe}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, Smad4 (SMAD family member 4) [NCBI Gene 17128] {aka D18Wsu70e, DPC4, Madh4}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, KCNK2 (potassium two pore domain channel subfamily K member 2) [NCBI Gene 3776] {aka K2p2.1, TPKC1, TREK, TREK-1, TREK1, hTREK-1c}, Egfr (epidermal growth factor receptor) [NCBI Gene 13649] {aka 9030024J15Rik, Erbb, Errb1, Errp, Wa5, wa-2}, Orai1 (ORAI calcium release-activated calcium modulator 1) [NCBI Gene 109305] {aka D730049H07Rik, Tmem142a, orai-1}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}, TMEM175 (transmembrane protein 175) [NCBI Gene 84286] {aka hTMEM175}, Atp4b (ATPase, H+/K+ exchanging, beta polypeptide) [NCBI Gene 11945], Gja1 (gap junction protein, alpha 1) [NCBI Gene 14609] {aka Cnx43, Cx43, Cx43alpha1, Cxnk1, Gja-1, Npm1}, SLC9A1 (solute carrier family 9 member A1) [NCBI Gene 6548] {aka APNH, LIKNS, NHE-1, NHE1, PPP1R143}, SLC4A4 (solute carrier family 4 member 4) [NCBI Gene 8671] {aka HNBC1, KNBC, NBC1, NBC2, NBCe1, NBCe1-A}, Cd247 (CD247 antigen) [NCBI Gene 12503] {aka 4930549J05Rik, A430104F18Rik, Cd3, Cd3-eta, Cd3-zeta, Cd3h}, Cd274 (CD274 antigen) [NCBI Gene 60533] {aka A530045L16Rik, B7h1, Pdcd1l1, Pdcd1lg1, Pdl1}, Slc4a4 (solute carrier family 4 (anion exchanger), member 4) [NCBI Gene 54403] {aka NBC, NBC1}, Atp4a (ATPase, H+/K+ exchanging, gastric, alpha polypeptide) [NCBI Gene 11944], Cdc42 (cell division cycle 42) [NCBI Gene 12540], Kras (Kras proto-oncogene, GTPase) [NCBI Gene 16653] {aka K-Ras, K-Ras 2, K-ras, Ki-ras, Kras-2, Kras2}, TRPC1 (transient receptor potential cation channel subfamily C member 1) [NCBI Gene 7220] {aka HTRP-1, TRP1}, Trp53 (transformation related protein 53) [NCBI Gene 22059] {aka Tp53, bbl, bfy, bhy, p44, p53}, Slc2a1 (solute carrier family 2 (facilitated glucose transporter), member 1) [NCBI Gene 20525] {aka GT1, Glut-1, Glut1, M100200, Rgsc200}, Hv1 (hepatitis virus (MHV-2) susceptibility) [NCBI Gene 107755] {aka Hv-1}, Ptprc (protein tyrosine phosphatase receptor type C) [NCBI Gene 19264] {aka B220, CD45R, Cd45, L-CA, Ly-5, Lyt-4}, mct1 (modifier of curly tail 1) [NCBI Gene 17236], Vsir (V-set immunoregulatory receptor) [NCBI Gene 74048] {aka 4632428N05Rik, Dies1, PD-1H, VISTA}, Kcnh1 (potassium voltage-gated channel, subfamily H (eag-related), member 1) [NCBI Gene 16510] {aka EAG1, Kv10.1, M-eag, mEAG1}, Yap1 (yes-associated protein 1) [NCBI Gene 22601] {aka Yap, Yap65, Yki, Yorkie}, Trpc6 (transient receptor potential cation channel, subfamily C, member 6) [NCBI Gene 22068] {aka LLHWJM002, LLHWJM003, LLHWJM004, TRP-6, Trrp6, mtrp6}, Asic1 (acid-sensing ion channel 1) [NCBI Gene 11419] {aka ASIC, ASIC1a, ASIC1b, Accn2, B530003N02Rik, BNaC2}, Tnfsf10 (tumor necrosis factor (ligand) superfamily, member 10) [NCBI Gene 22035] {aka A330042I21Rik, APO-2L, Ly81, TL2, Tnlg6a, Trail}, Piezo1 (piezo-type mechanosensitive ion channel component 1) [NCBI Gene 234839] {aka 9630020g22, Fam38a, mKIAA0233}, Ppara (peroxisome proliferator activated receptor alpha) [NCBI Gene 19013] {aka 4933429D07Rik, Nr1c1, PPAR-alpha, PPARalpha, Ppar}, Bcl2l1 (BCL2-like 1) [NCBI Gene 12048] {aka Bcl(X)L, Bcl-XL, Bcl2l, BclX, bcl-x, bcl2-L-1}
- **Diseases:** melanoma (MESH:D008545), fibrosis (MESH:D005355), PDAC (MESH:D021441), inflammatory diseases (MESH:D007249), Pancreatic Cancer (MESH:D010190), Lewis lung carcinoma cell tumors (MESH:D055752), Cancer (MESH:D009369), Pancreatic (MESH:D010195), hypoxic (MESH:D002534), hypoxia (MESH:D000860), metastasis (MESH:D009362), tumorigenicity (MESH:D002471), chronic pancreatitis (MESH:D050500), acidosis (MESH:D000138), breast cancer (MESH:D001943)
- **Chemicals:** CCX168 (MESH:C000620232), esomeprazole (MESH:D064098), Acid (MESH:D000143), lactate (MESH:D019344), alanine (MESH:D000409), luminal (MESH:D010634), HCl (MESH:D006851), NaOH (MESH:D012972), phosphoethanolamine (MESH:C005448), hyaluronan (MESH:D006820), Ca2+ (-), K+ (MESH:D011188), proton (MESH:D011522), LTB4 (MESH:D007975), amino acids (MESH:D000596), HCO3 - (MESH:D001639), fatty acid (MESH:D005227), erlotinib (MESH:D000069347), CO2 (MESH:D002245), glutamine (MESH:D005973), ATP (MESH:D000255), lipids (MESH:D008055), SLC-0111 (MESH:C000625353), pantoprazole (MESH:D000077402), H+ (MESH:D006859), cariporide (MESH:C093373), lysophosphatidylcholines (MESH:D008244), gemcitabine (MESH:D000093542), reactive oxygen species (MESH:D017382), glucose (MESH:D005947)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** R776H, R273H

## Full text

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## Figures

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## References

124 references — full list in the complete paper: https://tomesphere.com/paper/PMC12946857/full.md

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Source: https://tomesphere.com/paper/PMC12946857